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14511-59-2

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  • Ethyl 4-[2-(5-Chloro-2-methoxybenzamido)ethyl]benzene Sulfonamide Carbamate

    Cas No: 14511-59-2

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14511-59-2 Usage

Chemical Properties

Off-White Solid

Uses

An impurity arising in the synthesis of Glyburide (G598350).

Check Digit Verification of cas no

The CAS Registry Mumber 14511-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,1 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14511-59:
(7*1)+(6*4)+(5*5)+(4*1)+(3*1)+(2*5)+(1*9)=82
82 % 10 = 2
So 14511-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H21ClN2O6S/c1-3-28-19(24)22-29(25,26)15-7-4-13(5-8-15)10-11-21-18(23)16-12-14(20)6-9-17(16)27-2/h4-9,12H,3,10-11H2,1-2H3,(H,21,23)(H,22,24)

14511-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-[2-(5-Chloro-2-methoxybenzamido)ethyl]benzene Sulfonamide Carbamate

1.2 Other means of identification

Product number -
Other names [p-[2-(5-chloro-o-anisamido)ethyl]phenyl]sulfonyl]Carbamic 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:14511-59-2 SDS

14511-59-2Relevant articles and documents

Synthesis technology of glibenclamide

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Paragraph 0043; 0045, (2017/08/25)

The invention provides a novel synthesis technology of a glibenclamide bulk pharmaceuticals. The glibenclamide product is finally prepared by taking sulfamide as a starting raw material through the four steps of a secondary condensation reaction, a compounding reaction, a dealcoholization reaction and refining. The technology has the advantages of being high in yield, low in purity, easy and convenient to operate, suitable for industrialized production and the like.

SYNTHESIS OF 4-trans-BENZENESULFONYL>UREIDO>CYCLOHEXANOL HEMISUCCINATE ESTER

Stephon, Robert L.,Niedbala, R. Sam,Schray, Keith J.,Heindel, Ned D.

, p. 339 - 342 (2007/10/03)

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