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diiminosuccinonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28321-79-1

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28321-79-1 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 37, p. 4133, 1972 DOI: 10.1021/jo00798a037

Check Digit Verification of cas no

The CAS Registry Mumber 28321-79-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,2 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28321-79:
(7*2)+(6*8)+(5*3)+(4*2)+(3*1)+(2*7)+(1*9)=111
111 % 10 = 1
So 28321-79-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H2N4/c5-1-3(7)4(8)2-6/h7-8H/b7-3+,8-4+

28321-79-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethanediimidoyl dicyanide

1.2 Other means of identification

Product number -
Other names DISN

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:28321-79-1 SDS

28321-79-1Relevant articles and documents

Synthesis and spectral parameters of tetra(6-tert-butyl-2,3-quinoxalino) porphyrazine and its metal complexes

Efimova,Korzhenevskii,Koifman

, p. 1447 - 1451 (2008)

Tetra(6-tert-butyl-2,3-quinoxalino)porphyrazine and its complexes with bivalent metals were synthesized for the first time by template tetramerization of 6-tert-butylquinoxaline-2,3-dicarbonitrile. The obtained macrocyclic compounds are soluble in hydroph

Synthesis and spectral properties of octacyanopyrazinoporphyrazine and its metallocomplexes

Belozerova, Yu. I.,Efimova,Korzhenevskii,Koifman

, p. 2678 - 2684 (2009)

Octacyanopyrazinoporphyrazine was for first time synthesized by template tetramerization of tetracyanopyrazine, and its complexes with bivalent metals were prepared. The compounds obtained were characterized by MALDI-TOF mass spectral data, elemental anal

Synthesis and Investigation of 2,3,5,6-Tetra-(1H-tetrazol-5-yl)pyrazine Based Energetic Materials

Witkowski, Tomasz G.,Richardson, Paul,Gabidullin, Bulat,Hu, Anguang,Murugesu, Muralee

, p. 984 - 990 (2018)

The structures and properties of several energetic compounds based on a high-nitrogen-content anion, namely 2,3,5,6-tetra(1H-tetrazol-5-yl)pyrazine (H4TTP) are reported here for the first time. These energetic salts were synthesized by reacting H4TTP with various alkali metal hydroxides (sodium, potassium, rubidium, caesium) and N-based (ammonia, hydrazine, hydroxylamine, guanidine carbonate, aminoguanidine bicarbonate). The resulting materials were comprehensively characterized by multinuclear (1H, 13C) NMR spectroscopy, infrared spectroscopy, elemental analysis, DSC, as well as low-temperature single-crystal X-ray diffraction. Heats of formation for the metal-free species as well as detonation parameters were calculated. The presented energetic materials (EMs) show high thermal stability (207 °C≤Tdec≤300 °C), while the metal-free ionic derivatives exhibit desirable properties such as detonation velocity (6873 m s?1≤VC-J≤8364 m s?1), detonation pressure (14.3 GPa≤pC-J≤24.9 GPa), and specific impulse (141.4≤Isp≤192.5 s).

IRON AMINO COMPLEX AND METHOD OF PRODUCING THE SAME

-

Paragraph 0046, (2016/12/12)

PROBLEM TO BE SOLVED: To provide a novel iron amino complex, and a method of producing the same. SOLUTION: An iron amino complex is obtained by mixing an iron compound with a compound having two amino groups and two nitrile groups in solvent. COPYRIGHT: (C)2015,JPO&INPIT

Facile synthesis of hydrazine derivatives of 5H-pyrrolo[3,4-b]pyrazine and 1H-pyrrolo[3,4-b]quinoxaline

Hordiyenko, Olga V.,Rudenko, Igor V.,Zamkova, Irina A.,Denisenko, Oleksandr V.,Biitseva, Angelina V.,Arrault, Axelle,Tolmachev, Andrei A.

, p. 3375 - 3382 (2014/01/06)

A convenient and efficient route for the chemoselective synthesis of carbohydrazide, arenesulfonylhydrazide, and thiosemicarbazone derivatives of 5H-pyrrolo[3,4-b]pyrazine and 1H-pyrrolo[3,4-b]quinoxaline from the corresponding dinitriles and substituted hydrazines was elaborated. The synthesis of starting pyrazine-2,3-dicarbonitrile was sufficiently improved by using concentrated HCl as a catalyst. Georg Thieme Verlag Stuttgart . New York.

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