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1365271-76-6

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1365271-76-6 Usage

Physical State

White solid

Solubility

Insoluble in water, soluble in organic solvents

Uses

Versatile building block in organic synthesis, production of pharmaceuticals and agrochemicals, intermediate in the production of dyes, pigments, and specialty chemicals

Stability

Relatively stable

Toxicity

Low acute toxicity, but can be a skin and eye irritant

Handling

Should be handled with care

Check Digit Verification of cas no

The CAS Registry Mumber 1365271-76-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,5,2,7 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1365271-76:
(9*1)+(8*3)+(7*6)+(6*5)+(5*2)+(4*7)+(3*1)+(2*7)+(1*6)=166
166 % 10 = 6
So 1365271-76-6 is a valid CAS Registry Number.

1365271-76-6SDS

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 2-[4-(trifluoromethoxy)phenyl]benzonitrile

1.2 Other means of identification

Product number -
Other names 4'-trifluoromethoxy[1,1'-biphenyl]-2-carbonitrile

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:1365271-76-6 SDS

1365271-76-6Downstream Products

1365271-76-6Relevant articles and documents

Palladium-catalyzed desulfitative cross-coupling of sodium arylsulfinates with aryl bromides and chlorides: An alternative convenient synthesis of biaryls

Zhou, Chao,Li, Yaming,Lu, Yang,Zhang, Rong,Jin, Kun,Fu, Xinmei,Duan, Chunying

, p. 1269 - 1273 (2013/11/06)

An alternative method for synthesis of biaryls has been developed through the Pd catalyzed desulfitative coupling reaction of sodium arylsulfinates with aryl bromides and chlorides. The procedure tolerates a variety of functional groups, such as cyano, formyl, acetyl, chloro, methoxy, trifluoromethyl and heteroaromatic unit. The desired products were obtained in moderate to excellent yields under relatively mild reaction conditions without additives, base or co-catalyst. An alternative method for synthesis of biaryls has been developed through the Pd catalyzed desulfitative coupling reaction of sodium arylsulfinates with aryl bromides and chlorides. The procedure tolerates a variety of functional groups, such as cyano, formyl, acetyl, chloro, methoxy, trifluoromethyl and heteroaromatic unit. The desired products were obtained in moderate to excellent yields under relatively mild reaction conditions without additives, base or co-catalyst. Copyright

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