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3-Chloro-benzimidic acid ethyl ester is an organic compound with the chemical formula C10H10ClN2O2. It is a derivative of benzimidic acid, featuring a chlorine atom at the 3rd position and an ethyl ester group attached to the nitrogen atom. This white crystalline solid is soluble in organic solvents and is commonly used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical compounds. Its molecular structure consists of a benzene ring fused to an imidazole ring, with a chlorine atom attached to the benzene ring and an ethyl ester group connected to the nitrogen atom of the imidazole ring. The compound is known for its reactivity and can undergo various chemical transformations, making it a valuable building block in the synthesis of complex molecules.

827-64-5

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827-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 827-64-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 827-64:
(5*8)+(4*2)+(3*7)+(2*6)+(1*4)=85
85 % 10 = 5
So 827-64-5 is a valid CAS Registry Number.

827-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-chlorobenzenecarboximidate

1.2 Other means of identification

Product number -
Other names 3-CHLORO-BENZIMIDIC ACID ETHYL ESTER

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:827-64-5 SDS

827-64-5Relevant academic research and scientific papers

Rh(III)-Catalyzed [3 + 2] Annulation via C-H Activation: Direct Access to Trifluoromethyl-Substituted Indenamines and Aminoindanes

Chaudhary, Bharatkumar,Auti, Prashant,Shinde, Suchita Dattatray,Yakkala, Prasanna Anjaneyulu,Giri, Deepesh,Sharma, Satyasheel

supporting information, p. 2763 - 2767 (2019/04/30)

The rhodium(III)-catalyzed direct C-H addition and annulation of benzimidates and aldimines with β-(trifluoromethyl)-α,β-unsaturated ketones is described. This protocol provides the facile and efficient formation of various trifluoromethyl-containing inde

HETEROARYL INHIBITORS OF PDE4

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Paragraph 0555, (2014/05/24)

The present invention relates to compounds and methods useful as inhibitors of phosphodiesterase 4 (PDE4) for the treatment or prevention of disease.

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