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369-54-0

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369-54-0 Usage

Chemical Properties

clear colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 369-54-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 369-54:
(5*3)+(4*6)+(3*9)+(2*5)+(1*4)=80
80 % 10 = 0
So 369-54-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H6F3NS/c8-7(9,10)12-6-3-1-2-5(11)4-6/h1-4H,11H2

369-54-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Detail
  • TCI America

  • (T1774)  α,α,α',α'-Tetrafluoro-p-xylene  >98.0%(GC)

  • 369-54-0

  • 5g

  • 990.00CNY

  • Detail
  • TCI America

  • (T1774)  α,α,α',α'-Tetrafluoro-p-xylene  >98.0%(GC)

  • 369-54-0

  • 25g

  • 3,640.00CNY

  • Detail
  • Alfa Aesar

  • (B22193)  1,4-Bis(difluoromethyl)benzene, 98%   

  • 369-54-0

  • 1g

  • 262.0CNY

  • Detail
  • Alfa Aesar

  • (B22193)  1,4-Bis(difluoromethyl)benzene, 98%   

  • 369-54-0

  • 5g

  • 970.0CNY

  • Detail

369-54-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Bis(difluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names 1,4-BIS(DIFLUOROMETHYL)BENZENE

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:369-54-0 SDS

369-54-0Relevant articles and documents

Microwave-assisted synthesis of 1,4-bis(difluoromethyl)benzene

Pan, Dong-Hui,Wang, Tong-Zhen,Xiao, Guo-Min

, p. 1249 - 1254 (2017)

A fast, mild, and practical microwave-assisted protocol for synthesis of 1,4-bis(difluoromethyl)benzene from 1,4-bis(dichloromethyl)benzene and KF was developed. The new protocol increased the yield and reduced the reaction time significantly in contrast to the conventional heating procedure. Also, the synergistic effect of a composite phase transfer catalyst was studied.

Direct Difluoromethylation of Aryl Halides via Base Metal Catalysis at Room Temperature

Xu, Long,Vicic, David A.

supporting information, p. 2536 - 2539 (2016/03/12)

A stable and isolable difluoromethyl zinc reagent has been prepared through the reaction of ICF2H with diethyl zinc and DMPU. This new zinc reagent is a free-flowing solid and can be used in combination with a nickel catalyst to difluoromethylate aryl iodides, bromides, and triflates at room temperature. Such mild conditions for the catalytic difluoromethylation of these substrates are unprecedented.

Efficient synthesis of p-bis-(chlorodifluoromethyl)benzene

Dolbier Jr., William R.,Duan, Jian-Xin,Rong, Xiao X.

, p. 1091 - 1093 (2008/02/08)

Selective, high yield partial fluorination of p-bis-(trichloromethyl)benzene to p-bis-(chlorodifluoromethyl)benzene has been accomplished by warming a slurry of the p-bis-(trichloromethyl)benzene in anhydrous HF which also contains a small quantity of inert solvent, such as 1,2-dichloroethane.

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