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Benzene, (1,1-difluoroethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124382-13-4

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124382-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124382-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,8 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 124382-13:
(8*1)+(7*2)+(6*4)+(5*3)+(4*8)+(3*2)+(2*1)+(1*3)=104
104 % 10 = 4
So 124382-13-4 is a valid CAS Registry Number.

124382-13-4SDS

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 1,1-difluoroethoxybenzene

1.2 Other means of identification

Product number -
Other names Benzene,(1,1-difluoroethoxy)

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:124382-13-4 SDS

124382-13-4Downstream Products

124382-13-4Relevant academic research and scientific papers

Synthesis of aryl α,α-difluoroethyl thioethers a novel structure motif in organic chemistry, and extending to aryl α,α-difluoro oxyethers

Tomita, Ren,Al-Maharik, Nawaf,Rodil, Andrea,Bühl, Michael,O'Hagan, David

, p. 1113 - 1117 (2018/02/22)

A method for the preparation of aryl α,α-difluoroethyl thioethers (ArSCF2CH3) is reported and the synthesis approach is extended to aryl α,α-difluoroethyl oxygen ethers. Selected building blocks are further elaborated in cross-coupli

Reaction of carbonyl compounds with xenon difluoride in the presence of silicon tetrafluoride

Tamura, Masanori,Matsukawa, Yasuhisa,Quan, Heng-Dao,Mizukado, Junji,Sekiya, Akira

, p. 705 - 709 (2007/10/03)

Reaction of various carbonyl compounds with xenon difluoride in the presence of silicon tetrafluoride was investigated. Aromatic aldehyde, ketones, and α-ketoester react with xenon difluoride to give α,α-difluoroalkyl phenyl ethers. However, acid fluoride, ester, acid cyanide, α-ketocarboxylic acid, or thioester do not afford the corresponding products. In the case of cinnamaldehyde, fluorination was accompanied by intramolecular cyclization to afford fluorinated epoxide.

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