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36635-56-0

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36635-56-0 Usage

Synthesis Reference(s)

Tetrahedron Letters, 13, p. 2367, 1972 DOI: 10.1016/S0040-4039(01)85304-1

Check Digit Verification of cas no

The CAS Registry Mumber 36635-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,3 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36635-56:
(7*3)+(6*6)+(5*6)+(4*3)+(3*5)+(2*5)+(1*6)=130
130 % 10 = 0
So 36635-56-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO3S/c1-8-2-4-9(5-3-8)14(12,13)7-10-6-11/h2-6H,7H2,1H3,(H,10,11)

36635-56-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(4-methylphenyl)sulfonylmethyl]formamide

1.2 Other means of identification

Product number -
Other names F0749-0010

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:36635-56-0 SDS

36635-56-0Relevant articles and documents

Br?nsted Acid Organocatalyzed Three-Component Hydroamidation Reactions of Vinyl Ethers

Smajlagic, Ivor,Carlson, Brenden,Dudding, Travis

, p. 4171 - 4181 (2021)

Hydroamidation of carbon-carbon double bonds is an attractive strategy for installing nitrogen functionality into molecular scaffolds and, with it, increasing molecular complexity. To date, metal-based approaches have dominated this area of chemical synth

Phenyl pyrrole compound and application thereof in bactericidal activity

-

Paragraph 0137; 0139, (2020/08/17)

The invention provides a novel phenyl pyrrole compound, and the phenyl pyrrole compound shows good bactericidal activity and can be used for preparing a broad-spectrum plant bactericide. In addition,the synthesis route is simple, the operation is convenient, the synthesis cost is reduced, and ecological environment pollution to soil, surface water, underground water and the like is avoided.

A 2-fluoro-4-methyl sulfonyl methyl isonitriles method for the synthesis of

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Paragraph 0021; 0022, (2017/03/08)

The invention discloses a synthesis method of 2-fluoro-4-toluenesulfonylmethyl isocyanide. The method comprises the following steps: with sodium p-tolylsulfinate as a raw material, carrying out similar Mannich condensation and amide dehydration reaction to prepare tolylsulfonylmethyl isocyanide; adding a hydrofluoric acid aqueous solution and an Ni-CO catalyst to tolylsulfonylmethyl isocyanide; and fully reacting under nitrogen protection, and carrying out suction filtration, washing and drying to obtain faint yellow crystal 2-fluoro-4-toluenesulfonylmethyl isocyanide, wherein the yield reaches over 92%, and the purity is 99.8%. The synthesis method has the advantages of being available in reaction raw materials, mild in condition, high in yield, suitable for industrial production and the like.

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