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88210-30-4

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88210-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88210-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,1 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88210-30:
(7*8)+(6*8)+(5*2)+(4*1)+(3*0)+(2*3)+(1*0)=124
124 % 10 = 4
So 88210-30-4 is a valid CAS Registry Number.

88210-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-4-[(4-nitrophenyl)hydrazinylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 3.4'-Dinitro-4-oxy-azobenzol

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:88210-30-4 SDS

88210-30-4Downstream Products

88210-30-4Relevant articles and documents

AZOCOUPLING OF o-DINITROBENZENE: REACTIONS OF THE DIANION AND ANION-RADICAL WITH ARYLDIAZOCATIONS

Todres, Z. V.,Ovsepyan, G. Ts.,Ionina, E. A.,Kosnikov, A. Yu.,Lindeman, S. V.,Struchkov, Yu. T.

, p. 1651 - 1656 (2007/10/02)

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A Simple Route for the Synthesis of Chlorosubstituted Arylazobenzenes, Arylazonaphtalenes, and Arylazopyrazoles

Guenther, R.,Jaehne, E.,Hartmann, H.,Schulze, M.

, p. 945 - 954 (2007/10/02)

The reaction of arylazophenoles and arylazohydroxypyrazoles (or their tautomer hydrazones) 10, 11, and 15 with POCl3 in dimethylformamide yields chlorosubstituted arylazobenzenes or arylazopyrazoles 12, 13 and 16, resp., in moderate to high yields.The substitution of the OH-group by the Cl-moiety is favoured by acceptor substituents in the aryl fragments ortho- and/or para-linked to the azo group.In case that arylazocompounds derived from resorcinol are used the substitution reaction runs in a stepwise manner giving raise to the formation of o-hydroxy-p-chlorosubstit uted azo compounds 18 primarily and then of dichlorosubstituted azo compounds 19.

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