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660431-65-2

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660431-65-2 Usage

General Description

[1-(2-Fluorophenyl)-1-tosyl]methyl isocyanide is a chemical compound with the molecular formula C16H14FNO2S and a molecular weight of 305.35 g/mol. It is a tosylated isocyanide derivative with a fluorophenyl group attached to the carbon atom. [1-(2-FLUOROPHENYL)-1-TOSYL]METHYL ISOCYANIDE is commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals and bioactive compounds. It is known for its reactivity as a nucleophile and as a ligand in transition metal-catalyzed reactions. Due to its versatile applications in chemical research, [1-(2-Fluorophenyl)-1-tosyl]methyl isocyanide is a valuable and widely used compound in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 660431-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,0,4,3 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 660431-65:
(8*6)+(7*6)+(6*0)+(5*4)+(4*3)+(3*1)+(2*6)+(1*5)=142
142 % 10 = 2
So 660431-65-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H12FNO2S/c1-11-7-9-12(10-8-11)20(18,19)15(17-2)13-5-3-4-6-14(13)16/h3-10,15H,1H3

660431-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-fluoro-2-[isocyano-(4-methylphenyl)sulfonylmethyl]benzene

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:660431-65-2 SDS

660431-65-2Downstream Products

660431-65-2Relevant articles and documents

In silico-driven multicomponent synthesis of 4,5- and 1,5-disubstituted imidazoles as indoleamine 2,3-dioxygenase inhibitors

Fallarini,Massarotti,Gesù,Giovarruscio,Coda Zabetta,Bergo,Giannelli,Brunco,Lombardi,Sorba,Pirali

, p. 409 - 419 (2016/04/01)

Indoleamine 2,3-dioxygenase is involved in pathological immune escape and has recently become an attractive target for anti-cancer therapy. 4-Phenylimidazole (4-PI) provides a promising starting point for the development of IDO1 inhibitors. With the aim o

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