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75112-66-2

75112-66-2

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75112-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75112-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,1 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75112-66:
(7*7)+(6*5)+(5*1)+(4*1)+(3*2)+(2*6)+(1*6)=112
112 % 10 = 2
So 75112-66-2 is a valid CAS Registry Number.

75112-66-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-3-(4-nitroanilino)naphthalene-1,4-dione

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:75112-66-2 SDS

75112-66-2Relevant articles and documents

Thermolysis of 2-azido-3-(R-anilino)-1,4-naphthoquinones. Nitrene insertion versus hydrogen abstraction

Cárdenas-Chaparro, Agobardo,Leyva, Elisa,Loredo-Carrillo, Silvia E.,Martínez-Richa, Antonio,Platz, Matthew S.

, (2020/03/03)

2-chloro-3-(R-anilino)-1,4-naphthoquinones react with sodium azide upon refluxing in DMF. The thermochemistry of 2-azido-3-(R-anilino)-1,4-naphthoquinone is strongly modified by the substituent on aniline. Having an strong electron-donor like O-R results

Palladium-catalyzed amination of 2,3-dichloro-1,4-naphthoquinone with nitroarylamines

Wang, Xiao-Lei,Zheng, Xiu-Fang,Reiner, John

, p. 942 - 944 (2007/10/03)

A convenient one-step synthesis of 2-[(nitroaryl)amino]-3-chloro-1,4- naphthoquinones is reported. The direct amination of 2,3-dichloro-1,4- naphthoquinone with nitro-substituted aryl amines is catalyzed by PdCl 2(dppf)/dppf in the presence of

Synthesis and Structure of Chlorine-Containing 2-Amino-1,4-naphthoquinone Derivatives

Litvin, B. L.,Gubrii, Z. V.,Shermolovich, Yu. G.,Novikov, V. P.

, p. 377 - 383 (2007/10/03)

Exhaustive chlorination of 2-amino-1,4-naphthoquinone derivatives yields 3,3-dichloro-2-imino-2,3-dihydro-1,4-naphthoquinones.

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