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N-(PHENYLSULFONYLMETHYL)FORMAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28918-58-3

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28918-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28918-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,1 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28918-58:
(7*2)+(6*8)+(5*9)+(4*1)+(3*8)+(2*5)+(1*8)=153
153 % 10 = 3
So 28918-58-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO3S/c10-6-9-7-13(11,12)8-4-2-1-3-5-8/h1-6H,7H2,(H,9,10)

28918-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(benzenesulfonylmethyl)formamide

1.2 Other means of identification

Product number -
Other names Formamidomethyl-phenyl-sulfon

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:28918-58-3 SDS

28918-58-3Relevant academic research and scientific papers

Alkyl sulfinates: Formal nucleophiles for synthesizing TosMIC analogs

Lujan-Montelongo, J. Armando,Estevez, Angel Ojeda,Fleming, Fraser F.

, p. 1602 - 1605 (2015/03/04)

Alkyl sulfinates function as formal nucleophiles in Mannich-type reactions to give sulfonyl formamides, which are readily dehydrated to the corresponding sulfonylmethyl isonitriles. The efficient, two-step synthesis provides a general route to sulfonylmethyl isonitriles from readily available methyl sulfinates or thiols. Mechanistic analysis reveals that the unusual nucleophlicity of the alkyl sulfinates arises from the in situ release of sulfinic acids.

COMPOSITION, SYNTHESIS, AND USE OF NEW ARYLSULFONYL ISONITRILES

-

, (2015/09/23)

This invention relates to novel isonitriles, including arylsulfonyl isonitriles, and methods for their synthesis. The isonitriles include a conjugated ring system. The structure is designed with the flexibility to have multiple substitution patterns. The isonitriles may be used in applications including, but not limited to, pharmaceutical compositions.

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