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3-FORMYLBENZENESULFONYL CHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53460-88-1

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53460-88-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53460-88-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,6 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53460-88:
(7*5)+(6*3)+(5*4)+(4*6)+(3*0)+(2*8)+(1*8)=121
121 % 10 = 1
So 53460-88-1 is a valid CAS Registry Number.

53460-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-formylbenzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names 3-FORMYLBENZENE-1-SULFONYL CHLORIDE

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:53460-88-1 SDS

53460-88-1Downstream Products

53460-88-1Relevant academic research and scientific papers

Synthesis of 3-Formylbenzenesulfonyl Chloride Derivatives

Bao, Xuefei,Liu, Ziao,Liang, Xinjie,Song, Dake,Shi, Tao,Zhao, Xuan,Bao, Changshun,Chen, Guoliang

, p. 3165 - 3170 (2017/07/12)

A synthetic route to 3-formylbenzenesulfonyl chloride derivatives from the corresponding benzaldehydes has been developed. The key step in this procedure is the conversion of aldehyde bisulfite adducts to target compounds via a two-stage reaction in the presence of Na 2 SO 4. A series of 3-formylbenzenesulfonyl chloride derivatives were prepared by this method and identified by chemical derivatization method.

The Development of an Effective Synthetic Route of Belinostat

Bao, Xuefei,Song, Dake,Qiao, Xuejun,Zhao, Xuan,Chen, Guoliang

, p. 1482 - 1488 (2016/08/30)

A practical synthetic route of belinostat is reported. Belinostat was obtained via a five-step process starting from benzaldehyde and including addition reaction with sodium bisulfite, sulfochlorination with chlorosulfonic acid, sulfonamidation with aniline, Knoevenagel condensation, and the final amidation with hydroxylamine. Key to the strategy is the preparation of 3-formylbenzenesulfonyl chloride using an economical and practical protocol. The main advantages of the route include inexpensive starting materials and acceptable overall yield. The scale-up experiment was carried out to provide 169 g of belinostat with 99.6% purity in 33% total yield.

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