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38700-18-4

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38700-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38700-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,0 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38700-18:
(7*3)+(6*8)+(5*7)+(4*0)+(3*0)+(2*1)+(1*8)=114
114 % 10 = 4
So 38700-18-4 is a valid CAS Registry Number.

38700-18-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name benzene-1,2,3-tricarbonitrile

1.2 Other means of identification

Product number -
Other names Benzol-1.2.3-tricarbonitril

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:38700-18-4 SDS

38700-18-4Downstream Products

38700-18-4Relevant articles and documents

Weak C - H ... N≡ C hydrogen bonds in the structures of two poly(cyano)-substituted ring systems

Jones, Peter G.,Hopf, Henning,Mlynek, Cornelia,Swaminathan, Vijay Narayanan

, p. o723-o725 (2008/09/18)

In benzene-1,2,3-tricarbonitrile, C9H3N3, the packing of the two independent mol-ecules is three-dimensional and complex, involving inter alia bifurcated (C - H)2...N systems from neighbouring CH groups. In [2.2]paracyclo-phane-4,5,12,13-tetra-carbonitrile, C20H12N4, the [2.2]paracyclo-phane systems display the usual distortions, namely lengthened C - C bonds and widened sp 3 angles in the bridges, narrow angles in the six-membered rings at the bridgehead atoms, and flattened boat conformations of the rings. The mol-ecules are linked by a series of C - H...N inter-actions to form layers parallel to the ab plane. International Union of Crystallography 2007.

Process for the preparation of 1,2,3-tricyanobenzene, phthalocyanines which are obtainable from 1,2,3-tricyanobenzene, and their use as pigments

-

, (2008/06/13)

1,2,3-Tricyanobenzene can be prepared in a good yield from fluorobenzonitriles by reaction with an alkali metal cyanide. This product can be converted into metal-free tetracyanophthalocyanines or into the corresponding metal complexes by tetramerisation,

Aromatic Nitro-group Displacement Reactions. Part 4. The Action of Cyanide and Halide Ions on Compounds containing Strongly Activated Nitro-groups

Gorvin, John H.

, p. 1831 - 1851 (2007/10/02)

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