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35042-99-0

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35042-99-0 Usage

Uses

Difluoromethyl 2,2,3,3-Tetrafluoropropyl Ether is a a component of refrigerant fluids.

Check Digit Verification of cas no

The CAS Registry Mumber 35042-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,4 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35042-99:
(7*3)+(6*5)+(5*0)+(4*4)+(3*2)+(2*9)+(1*9)=100
100 % 10 = 0
So 35042-99-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H4F6O/c5-2(6)4(9,10)1-11-3(7)8/h2-3H,1H2

35042-99-0 Well-known Company Product Price

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  • TCI America

  • (D4472)  Difluoromethyl 2,2,3,3-Tetrafluoropropyl Ether  >98.0%(GC)

  • 35042-99-0

  • 1g

  • 480.00CNY

  • Detail
  • TCI America

  • (D4472)  Difluoromethyl 2,2,3,3-Tetrafluoropropyl Ether  >98.0%(GC)

  • 35042-99-0

  • 5g

  • 1,650.00CNY

  • Detail

35042-99-0SDS

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 Difluoromethyl 2,2,3,3-tetrafluoropropyl ether

1.2 Other means of identification

Product number -
Other names Difluoromethyl 2,2,3,3-Tetrafluoropropyl Ether

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:35042-99-0 SDS

35042-99-0Downstream Products

35042-99-0Relevant articles and documents

Reactions of aliphatic fluoro-alcohols with CHClF2 at atmospheric pressure

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

, p. 400 - 404 (2007/10/03)

The reactions of aliphatic fluoro-alcohols with chlorodifluoromethane (CHClF2) at atmospheric pressure were examined. In the reaction of CF3CF2CH2OH, the difluoromethylated ether was obtained in moderate yield by using ethers such as 1,4-dioxane, diglyme and THF, or their mixtures with water as a reaction solvent. While acetal and orthoformate were also produced, the selectivity of the difluoromethylated ether could be improved by adding water to the reaction. The effect of water could be explained by the reaction mechanism.

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