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51327-24-3

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51327-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51327-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,2 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51327-24:
(7*5)+(6*1)+(5*3)+(4*2)+(3*7)+(2*2)+(1*4)=93
93 % 10 = 3
So 51327-24-3 is a valid CAS Registry Number.

51327-24-3SDS

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 1-(4-methoxyphenyl)sulfonyl-3-phenylurea

1.2 Other means of identification

Product number -
Other names Acetohexamid

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:51327-24-3 SDS

51327-24-3Downstream Products

51327-24-3Relevant articles and documents

A sulfonyl urea, sulfonamide ethyl ester preparation method of compound (by machine translation)

-

Paragraph 0094; 0100-0104; 0110-0115, (2017/08/02)

The description relates to a compound of formula (I) compound of the preparation method, wherein formula (II) with a compound represented by formula (III) as shown in the catalysis of palladium catalyst, under a carbon monoxide atmosphere, reacts in a solvent to obtain the compound. The invention related to the method of the reaction do not require strict-free conditions, does not need a high pressure carbon monoxide atmosphere, convenient and simple to operate, to a functional group and has very high power density and universality, the catalyst consumption is very small, the cost of reaction is very low, and can be widely used for preparing sulfonyl urea compound. R1 - SO2 - NH - CO - X (R3 )n - R2 (I) R1 - SO2 - R4 (II) HX (R3 )n - R2 (III) wherein X is O or N; n is 0 or 1; when X is when O, n=0; when X is when N, n=1; R1 Selected from aryl, heteroaryl, alkyl, alkenyl or alkynyl; R2 Selected from aryl, heteroaryl, alkyl, alkenyl or alkynyl; R3 Is selected from H, R2 , Or R3 And R2 A ring of connection; R4 For N3 Or a halogen atom; when R4 For nails halogen original, system also comprises a sodium azide. (by machine translation)

A convenient synthesis of sulfonylureas from carboxylic acids and sulfonamides via an in situ Curtius rearrangement

Luckhurst, Christopher A.,Millichip, Ian,Parker, Beth,Reuberson, James,Furber, Mark

, p. 8878 - 8882 (2008/03/14)

A one-pot reaction of carboxylic acids with sulfonamides to afford sulfonylureas is described.

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