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245539-09-7

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245539-09-7 Usage

General Description

1,2-Dichloro-3-isocyanobenzene is a chemical compound with the molecular formula C7H3Cl2NO. It is a yellow to brown colored solid that is used in the production of various chemical products, including pesticides and pharmaceuticals. 1,2-DICHLORO-3-ISOCYANOBENZENE is a derivative of benzene, with two chlorine atoms and an isocyanide functional group attached to the benzene ring. It is primarily used as an intermediate in the synthesis of other organic chemicals and is not commonly found in consumer products. 1,2-Dichloro-3-isocyanobenzene is considered to be a hazardous substance and must be handled with proper safety precautions due to its potential toxicity and environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 245539-09-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,5,3 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 245539-09:
(8*2)+(7*4)+(6*5)+(5*5)+(4*3)+(3*9)+(2*0)+(1*9)=147
147 % 10 = 7
So 245539-09-7 is a valid CAS Registry Number.

245539-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-DICHLORO-3-ISOCYANOBENZENE

1.2 Other means of identification

Product number -
Other names Phenyl isocyanide,2,3-dichloro

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:245539-09-7 SDS

245539-09-7Relevant articles and documents

Silver-Catalyzed Chemoselective [4+2] Annulation of Two Isocyanides: A General Route to Pyridone-Fused Carbo- and Heterocycles

Hu, Zhongyan,Dong, Jinhuan,Men, Yang,Lin, Zhichen,Cai, Jinxiong,Xu, Xianxiu

supporting information, p. 1805 - 1809 (2017/02/05)

A silver-catalyzed chemoselective [4+2] annulation of aryl and heteroaryl isocyanides with α-substituted isocyanoacetamides was developed for the facile and efficient synthesis of 2-aminoquinolones, naphthyridines, and phenanthrolines. A mechanism for this multistep domino reaction is proposed on the basis of a13C-labeling experiment, according to which an unprecedented chemoselective heterodimerization of two different isocyanides generates an α-amidoketenimine intermediate, which undergoes 1,3-amino migration to form an α-imidoylketene, followed by 6 π electrocyclization.

Process for the preparation of aryl isocyanide-dichlorides

-

, (2008/06/13)

An improved process for preparation of arylisocyanide dichloride by chlorinating N-arylformamide in the presence of thionyl chloride wherein the improvement comprises preparing the N-arylformamide by formylation of an arylamine having 6 to 12 aryl carbon

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