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130612-84-9

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130612-84-9 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 60, p. 3459, 1995 DOI: 10.1021/jo00116a037

Check Digit Verification of cas no

The CAS Registry Mumber 130612-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,1 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 130612-84:
(8*1)+(7*3)+(6*0)+(5*6)+(4*1)+(3*2)+(2*8)+(1*4)=89
89 % 10 = 9
So 130612-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H6FNS/c9-8(6-10)11-7-4-2-1-3-5-7/h1-5,8H

130612-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Fluoro(phenylthio)acetonitrile

1.2 Other means of identification

Product number -
Other names 2-fluoro-2-phenylsulfanylacetonitrile

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:130612-84-9 SDS

130612-84-9Upstream product

130612-84-9Downstream Products

130612-84-9Relevant articles and documents

Anodic fluorination based on cation exchange between alkali-metal fluorides and solid-supported acids

Tajima, Toshiki,Nakajima, Atsushi,Doi, Yuta,Fuchigami, Toshio

, p. 3550 - 3552 (2008/03/12)

(Chemical Equation Presented) Positively shocking: The interchange of cations between alkali-metal fluorides and solid-supported acids (see picture) in an electrolytic system promotes the anodic fluorination of organic compounds to give the corresponding

Electrolytic Partial Fluorination of Organic Compounds. 23.1 Regioselective Anodic Difluorination of Sulfides Using Novel Fluorine Source Et4NF·4HF

Konno, Akinori,Fuchigami, Toshio

, p. 8579 - 8581 (2007/10/03)

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Electrolytic Partial Fluorination of Organic Compounds. Regioselective Anodic Monofluorination of Organosulfur Compounds

Fuchigami, Toshio,Shimojo, Moriyasu,Konno, Akinori,Nakagawa, Kiyono

, p. 6074 - 6075 (2007/10/02)

Regioselective anodic monofluorination of aryl 2,2,2-trifluoroethyl sulfides gave, exclusively, aryl 1,2,2,2-tetrafluoroethyl sulfides, the products of fluorination at the position α to the trifluoromethyl group.The α-monofluorination of sulfides bearing

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