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CAS

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4,5-Dicyano-2-aminoimidazole is an organic compound with the chemical formula C4H2N6. It is characterized by the presence of two cyano groups (-CN) at the 4 and 5 positions and an amino group (-NH2) at the 2 position of the imidazole ring. 4,5-Dicyano-2-aminoimidazole has potential applications in various fields due to its unique chemical properties.

40953-34-2

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40953-34-2 Usage

Uses

Used in Organic Electronics Industry:
4,5-Dicyano-2-aminoimidazole is used as a key component in the fabrication of organic electrical bistable devices. These devices consist of a thin metal layer embedded within the organic material, which can be fabricated using a vacuum evaporation method. 4,5-Dicyano-2-aminoimidazole's unique electronic properties make it suitable for creating devices with the nominal layer structure of organic/metal-nanocluster/organic interposed between two electrodes.

Check Digit Verification of cas no

The CAS Registry Mumber 40953-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,5 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40953-34:
(7*4)+(6*0)+(5*9)+(4*5)+(3*3)+(2*3)+(1*4)=112
112 % 10 = 2
So 40953-34-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H3N5/c6-1-3-4(2-7)10-5(8)9-3/h(H3,8,9,10)

40953-34-2 Well-known Company Product Price

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  • Aldrich

  • (376744)  2-Amino-4,5-imidazoledicarbonitrile  97%

  • 40953-34-2

  • 376744-10G

  • 472.68CNY

  • Detail
  • Aldrich

  • (376744)  2-Amino-4,5-imidazoledicarbonitrile  97%

  • 40953-34-2

  • 376744-50G

  • 1,925.82CNY

  • Detail

40953-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-Dicyano-2-Aminoimidazole

1.2 Other means of identification

Product number -
Other names 2-amino-1H-imidazole-4,5-dicarbonitrile

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:40953-34-2 SDS

40953-34-2Relevant articles and documents

2-imidazol(in)e substituted aryl-1,2,3-triazole pesticides

-

, (2008/06/13)

Compounds of formula I STR1 and salts thereof, in which Ar, W, Z, A, R1-7, Y, m, p and n have the meanings given in the description, have pesticidal activity especially against insects, acarids and animal endoparasites.

Reactivity of Carbenes and Related Compounds towards Molecular Nitrogen

Grieve, Duncan M. A.,Lewis, Graham E.,Ravenscroft, Michael D.,Skrabal, Peter,Sonoda, Takaaki,et al.

, p. 1427 - 1443 (2007/10/02)

The thermal N2 exchange of a number of 15N-labelled diazo compounds was studied in solution.The compounds involved were 3-diazo-1-methylindolin-2-one (1), 9-diazafluorene (2), 5-diazo-1,3-cyclopentadiene-1,2,3,4-tetracarbonitrile (3), 2-diazo-2H-imidazole-4,5-dicarbonitrile (4), 4-diazocyclohexa-2,5-dienone (5), and the conjugate acids of 4 and 5, namely 4,5-dicyano-1H-imidazole-2-diazonium ion (6) and 4-hydroxybenzenediazonium ion (7).Only 1, 4, 6, and 7 exchange their diazo group with 'external' molecular N2.The results are explained on the hypothesis that only organic species which have an empty ? orbital and which are effective in ? electron back-donation are able to react with N2.Thus, reaction with carbenes is likely to occur only if the carbene is in the 1A2 singlet state and if its electrophilicity is high.

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