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Carbamic acid, [6-chloro-2-(phenylamino)-3-pyridinyl]-, ethyl ester, also known as ethyl 6-chloro-2-(phenylamino)-3-pyridinecarbamate, is a chemical compound with the molecular formula C13H12ClN3O2. It is a derivative of carbamic acid, featuring a 6-chloro-2-(phenylamino)-3-pyridinyl group attached to the carbamic acid backbone. Carbamic acid, [6-chloro-2-(phenylamino)-3-pyridinyl]-, ethyl ester is an ester, with an ethyl group (C2H5) esterifying the carbamic acid moiety. It is a white to off-white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound is known for its potential applications in the development of pesticides and other chemical products, highlighting its importance in the chemical industry.

6604-50-8

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6604-50-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6604-50-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,0 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6604-50:
(6*6)+(5*6)+(4*0)+(3*4)+(2*5)+(1*0)=88
88 % 10 = 8
So 6604-50-8 is a valid CAS Registry Number.

6604-50-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-(2-anilino-6-chloropyridin-3-yl)carbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid,[6-chloro-2-(phenylamino)-3-pyridinyl]-,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:6604-50-8 SDS

6604-50-8Relevant academic research and scientific papers

Compounds with antiulcer and antisecretory activity. III. N-substituted imidazolones condensed with nitrogen-containing heteroaromatic rings

Bianchi,Butti,Rossi,et al.

, p. 501 - 506 (2007/10/02)

The syntheses of imidazo[4,5-b]pyridin-2-ones and -thiones, imidazo [4,5-c]pyridin-2-ones and 7,9-dihydro-8H-purin-8-ones arylated (or heteroarylated) at an imidazolone nitrogen are reported. Only some compounds of the first series have marked antisecreto

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