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5664-79-9

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5664-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5664-79-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5664-79:
(6*5)+(5*6)+(4*6)+(3*4)+(2*7)+(1*9)=119
119 % 10 = 9
So 5664-79-9 is a valid CAS Registry Number.

5664-79-9SDS

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 4,6-dichloro-N-[4-[(4-nitrophenyl)diazenyl]phenyl]-1,3,5-triazin-2-amine

1.2 Other means of identification

Product number -
Other names -

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:5664-79-9 SDS

5664-79-9Downstream Products

5664-79-9Relevant articles and documents

Dye compound as well as preparation method and application thereof

-

Paragraph 0038; 0040-0043; 0055-0060; 0072-0077, (2019/07/01)

The invention discloses a dye compound. The structural formula of the compound is shown as a formula (I). The invention particularly relates to a dye compound as well as a preparation method and application thereof, and belongs to the technical field of t

Nucleophilic Substitutions in 1,3,5-Triazines. VII. The Kinetic and Mechanism of Cyanuric Chloride with 4'-Substituted 4-Aminoazobenzens

Havlik, I.,Bacaloglu, R.

, p. 936 - 942 (2007/10/02)

The kinetic and mechanism of cyanuric chloride reaction with 4'-substituted 4-aminoazobenzens in dioxan-water was studied by conductometry.An addition-elimination mechanism with a monomolecular elimination of chlorine ion at low water concentrations or a

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