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10254-60-1

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10254-60-1 Usage

General Description

N-(4-Fluorophenyl)-N-methylthiocarbamoyl chloride is a chemical compound with the molecular formula C8H8ClFNO. It is a chlorinated thioisocyanate derivative that is used in the synthesis of organic compounds. It is a white solid at room temperature and is insoluble in water but soluble in organic solvents. It is primarily used as a building block in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. N-(4-FLUOROPHENYL)-N-METHYLTHIOCARBAMOYL CHLORIDE is also known to be potentially hazardous and should be handled with care by trained professionals in a controlled laboratory environment.

Check Digit Verification of cas no

The CAS Registry Mumber 10254-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,5 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10254-60:
(7*1)+(6*0)+(5*2)+(4*5)+(3*4)+(2*6)+(1*0)=61
61 % 10 = 1
So 10254-60-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClFNS/c1-11(8(9)12)7-4-2-6(10)3-5-7/h2-5H,1H3

10254-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-fluorophenyl)-N-methylcarbamothioyl chloride

1.2 Other means of identification

Product number -
Other names N-Methyl-N-<4-fluor-phenyl>-thiocarbamylchlorid

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:10254-60-1 SDS

10254-60-1Relevant articles and documents

Tertiary thiols from allylic thiocarbamates by tandem enantioselective [3,3]-sigmatropic rearrangement and stereospecific arylation

Mingat, Gaelle,Maclellan, Paul,Laars, Marju,Clayden, Jonathan

, p. 1252 - 1255 (2014/03/21)

The synthesis of tertiary thiols in enantiomerically enriched form is accomplished by lithiation of enantiomerically enriched N-aryl allylic thiocarbamates. Formation of an allyllithium derivative promotes intramolecular N to C aryl migration to the posit

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