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1,3,5,7-Adamantanetetracarboxylic acid is a rigid, polycyclic carboxylic acid with the molecular formula C14H20O8, derived from the adamantane structure. It is known for its ability to form metal-organic frameworks (MOFs) due to its four carboxylic acid groups that can coordinate with metal ions to create stable coordination polymers. 1,3,5,7-ADAMANTANETETRACARBOXYLIC ACID is also recognized for its potential applications in drug delivery, catalysis, supramolecular chemistry, and nanotechnology, making it a versatile molecule of interest in various scientific and industrial fields.

100884-80-8

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100884-80-8 Usage

Uses

Used in Materials Science:
1,3,5,7-Adamantanetetracarboxylic acid is used as a building block for metal-organic frameworks (MOFs) for its ability to coordinate with metal ions, forming stable coordination polymers that are valuable in various applications such as gas storage, catalysis, and sensor technology.
Used in Drug Delivery Systems:
In the pharmaceutical industry, 1,3,5,7-Adamantanetetracarboxylic acid is utilized as a component in drug delivery systems due to its capacity to form hydrogen bonds with other molecules, which can enhance the solubility and bioavailability of drugs.
Used in Catalysis:
1,3,5,7-Adamantanetetracarboxylic acid serves as a catalyst or a catalyst support in chemical reactions, capitalizing on its structural properties to facilitate or enhance the reaction process.
Used in Supramolecular Chemistry:
In supramolecular chemistry, 1,3,5,7-Adamantanetetracarboxylic acid is employed for constructing complex molecular architectures and systems, taking advantage of its ability to form non-covalent interactions such as hydrogen bonding.
Used in Nanotechnology:
1,3,5,7-Adamantanetetracarboxylic acid is used in nanotechnology for the development of nanoscale materials and devices, leveraging its unique structural properties to create novel functional systems at the nanoscale.

Check Digit Verification of cas no

The CAS Registry Mumber 100884-80-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,8 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100884-80:
(8*1)+(7*0)+(6*0)+(5*8)+(4*8)+(3*4)+(2*8)+(1*0)=108
108 % 10 = 8
So 100884-80-8 is a valid CAS Registry Number.

100884-80-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name adamantane-1,3,5,7-tetracarboxylic acid

1.2 Other means of identification

Product number -
Other names 1,3,5,7-Adamantanetetracarboxylicacid (6CI)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:100884-80-8 SDS

100884-80-8Relevant articles and documents

Three-Dimensional Tetrathiafulvalene-Based Covalent Organic Frameworks for Tunable Electrical Conductivity

Chang, Jianhong,Fang, Qianrong,Guan, Xinyu,Li, Cuiyan,Li, Daohao,Li, Hui,Li, Shanshan,Qiu, Shilun,Tang, Lingxue,Valtchev, Valentin,Xue, Ming,Yan, Yushan

, (2019)

The functionalization of three-dimensional (3D) covalent organic frameworks (COFs) is essential to broaden their applications. However, the introduction of organic groups with electroactive abilities into 3D COFs is still very limited. Herein we report the first case of 3D tetrathiafulvalene-based COFs (3D-TTF-COFs) with non- or 2-fold interpenetrated pts topology and tunable electrochemical activity. The obtained COFs show high crystallinity, permanent porosity, and large specific surface area (up to 3000 m2/g). Furthermore, these TTF-based COFs are redox active to form organic salts that exhibit tunable electric conductivity (as high as 1.4 × 10-2 S cm-1 at 120 °C) by iodine doping. These results open a way toward designing 3D electroactive COF materials and promote their applications in molecular electronics and energy storage.

Cascade Polymers: Synthesis and Characterization of Four-Directional Spherical Dendritic Macromolecules Based on Adamantane

Newkome, George R.,Nayak, Ashutosh,Behera, Rajani K.,Moorefield, Charles N.,Baker, Gregory R.

, p. 358 - 362 (1992)

The syntheses and spectral characteristics of four-directional spherical dendritic macromolecules utilizing an adamantane core have been described.The dendrimer syntheses utilized 4-amino-4-(3-acetoxypropyl)-1,7-diacetoxyheptane or di-tert-butyl 4-amino-2-heptanedioate as the key building block.An improved synthetic procedure to 1,3,5,7-adamantanetetracarboxylic acid is reported.

A MOF-based Ultra-Strong Acetylene Nano-trap for Highly Efficient C2H2/CO2 Separation

Niu, Zheng,Cui, Xili,Pham, Tony,Verma, Gaurav,Lan, Pui Ching,Shan, Chuan,Xing, Huabin,Forrest, Katherine A.,Suepaul, Shanelle,Space, Brian,Nafady, Ayman,Al-Enizi, Abdullah M.,Ma, Shengqian

, p. 5283 - 5288 (2021)

Porous materials with open metal sites have been investigated to separate various gas mixtures. However, open metal sites show the limitation in the separation of some challenging gas mixtures, such as C2H2/CO2. Herein, we propose a new type of ultra-strong C2H2 nano-trap based on multiple binding interactions to efficiently capture C2H2 molecules and separate C2H2/CO2 mixture. The ultra-strong acetylene nano-trap shows a benchmark Qst of 79.1 kJ mol?1 for C2H2, a record high pure C2H2 uptake of 2.54 mmol g?1 at 1×10?2 bar, and the highest C2H2/CO2 selectivity (53.6), making it as a new benchmark material for the capture of C2H2 and the separation of C2H2/CO2. The locations of C2H2 molecules within the MOF-based nanotrap have been visualized by the in situ single-crystal X-ray diffraction studies, which also identify the multiple binding sites accountable for the strong interactions with C2H2.

Rigid multivalent scaffolds based on adamantane

Nasr, Khaled,Pannier, Nadine,Frangioni, John V.,Maison, Wolfgang

, p. 1056 - 1060 (2008)

(Chemical Equation Presented) We present two new synthetic strategies to rigid multivalent scaffolds of the general structure 1 based on adamantane. Both routes start from arylated adamantane derivatives and give the target compounds 12 and 18 in 5 and 7 steps, respectively. These scaffolds have been designed for the assembly of multivalent binders for cell surface epitopes. The adamantane nucleus exposes three carboxylic acid groups in a well-defined tripodal geometry for conjugation of targeting ligands. In addition, an amino group at the fourth bridgehead position provides a flexible linker for attachment of effector molecules such as contrast agents, radiotracers, or cytotoxins without interfering with the cell binding process.

3D microporous base-functionalized covalent organic frameworks for size-selective catalysis

Fang, Qianrong,Gu, Shuang,Zheng, Jie,Zhuang, Zhongbin,Qiu, Shilun,Yan, Yushan

, p. 2878 - 2882 (2014)

The design and synthesis of 3D covalent organic frameworks (COFs) have been considered a challenge, and the demonstrated applications of 3D COFs have so far been limited to gas adsorption. Herein we describe the design and synthesis of two new 3D microporous base-functionalized COFs, termed BF-COF-1 and BF-COF-2, by the use of a tetrahedral alkyl amine, 1,3,5,7-tetraaminoadamantane (TAA), combined with 1,3,5-triformylbenzene (TFB) or triformylphloroglucinol (TFP). As catalysts, both BF-COFs showed remarkable conversion (96 % for BF-COF-1 and 98 % for BF-COF-2), high size selectivity, and good recyclability in base-catalyzed Knoevenagel condensation reactions. This study suggests that porous functionalized 3D COFs could be a promising new class of shape-selective catalysts.

Chromophore Multiplication To Enable Exciton Delocalization and Triplet Diffusion Following Singlet Fission in Tetrameric Pentacene

Hetzer, Constantin,Basel, Bettina S.,Kopp, Sebastian M.,Hampel, Frank,White, Fraser J.,Clark, Timothy,Guldi, Dirk M.,Tykwinski, Rik R.

, p. 15263 - 15267 (2019)

A tetrameric pentacene, PT, has been used to explore the effects of exciton delocalization on singlet fission (SF). For the first time, triplet decorrelation through intramolecular triplet diffusion was observed following SF. Transient absorption spectros

Photochemical Carbonylation of Adamantanes; Simple Synthesis of 1,3,5,7-Tetracarbomethoxyadamantane

Bashir-Hashemi, A.,Li, Jianchang,Gelber, Nathan

, p. 1233 - 1236 (1995)

1,3,5,7-tetracarbomethoxyadamantane was obtained in one pot from the irradiation of a mixture of 1-adamantanecarboxylic and oxalyl chloride followed by methanolysis.

Self-Adjusting Metal–Organic Framework for Efficient Capture of Trace Xenon and Krypton

Al-Enizi, Abdullah M.,Fan, Ziwen,Forrest, Katherine A.,Ma, Shengqian,Niu, Zheng,Pham, Tony,Space, Brian,Thallapally, Praveen K.,Verma, Gaurav

supporting information, (2022/02/01)

The capture of the xenon and krypton from nuclear reprocessing off-gas is essential to the treatment of radioactive waste. Although various porous materials have been employed to capture Xe and Kr, the development of high-performance adsorbents capable of trapping Xe/Kr at very low partial pressure as in the nuclear reprocessing off-gas conditions remains challenging. Herein, we report a self-adjusting metal-organic framework based on multiple weak binding interactions to capture trace Xe and Kr from the nuclear reprocessing off-gas. The self-adjusting behavior of ATC-Cu and its mechanism have been visualized by the in-situ single-crystal X-ray diffraction studies and theoretical calculations. The self-adjusting behavior endows ATC-Cu unprecedented uptake capacities of 2.65 and 0.52 mmol g?1 for Xe and Kr respectively at 0.1 bar and 298 K, as well as the record Xe capture capability from the nuclear reprocessing off-gas. Our work not only provides a benchmark Xe adsorbent but proposes a new route to construct smart materials for efficient separations.

Rigid C3-symmetric scaffolds based on adamantane

Pannier, Nadine,Maison, Wolfgang

experimental part, p. 1278 - 1284 (2009/04/07)

Efficient syntheses of rigid C3-symmetric scaffolds based on adamantane are described. The scaffolds are available in multigram quantities and have been designed for conjugation to various natural products such as carbohydrates and peptides. Th

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