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2666-65-1

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2666-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2666-65-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,6 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2666-65:
(6*2)+(5*6)+(4*6)+(3*6)+(2*6)+(1*5)=101
101 % 10 = 1
So 2666-65-1 is a valid CAS Registry Number.

2666-65-1SDS

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 N-(4-bromophenyl)-1,1-dichloromethanimine

1.2 Other means of identification

Product number -
Other names (4-Brom-phenyl)-imidokohlensaeure-dichlorid

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:2666-65-1 SDS

2666-65-1Relevant articles and documents

Synthetic method of N-dichloromethylene aniline derivative

-

Paragraph 0039; 0040; 0041; 0042, (2017/08/27)

The invention discloses a synthetic method of an N-dichloromethylene aniline derivative represented by the formula II, wherein the synthesis method comprises the steps: with an isonitrile compound represented by the formula I as a raw material, in an organic solvent and under an action of iodobenzene dichloride represented by the formula III, carrying out a stirring reaction at the temperature of 0-50 DEG for 0.5-5 hours, and after the reaction is finished, separating and purifying the reaction liquid to obtain the N-dichloromethylene aniline derivative represented by the formula II. The synthetic method has the advantages of small toxicity of a chlorine source, environmental friendliness, mild reaction conditions, good universality of functional groups, convenience in operation and the like.

Methyl n-aryl-n-formyldithiocarbamates and fluorination thereof

Petko,Yagupol'skii

, p. 1173 - 1177 (2007/10/03)

By reaction of unsubstituted and substituted in the benzene ring formanilides with carbon disulfide and potassium hydroxide in dimethylformamide followed by methylation with methyl iodide were prepared methyl N-aryl-N-formyldithiocarbamates. The reaction of methyl N-4-bromophenyl-N-formyldithiocarbamate with SF4 furnished 4-bromo-N-difluorornethyl-N-trifluoromethylaniline.

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