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357-28-8

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357-28-8 Usage

General Description

1,1,1,2,2-pentafluoro-4-methyl-pentan-3-one is a chemical compound with the molecular formula C6H5F5O. It is a clear, colorless liquid with a slightly fruity odor, and it is commonly used as a solvent. This chemical is also known for its low toxicity and high stability, making it a popular choice for industrial and laboratory applications. It is also used in the production of pharmaceuticals, agricultural chemicals, and other specialty chemicals. Additionally, 1,1,1,2,2-pentafluoro-4-methyl-pentan-3-one is known for its low environmental impact, and it is not considered to be a volatile organic compound.

Check Digit Verification of cas no

The CAS Registry Mumber 357-28-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 357-28:
(5*3)+(4*5)+(3*7)+(2*2)+(1*8)=68
68 % 10 = 8
So 357-28-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H7F5O/c1-3(2)4(12)5(7,8)6(9,10)11/h3H,1-2H3

357-28-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,2,2-pentafluoro-4-methylpentan-3-one

1.2 Other means of identification

Product number -
Other names 1,1,1,2,2-PENTAFLUORO-4-METHYL-PENTAN-3-ONE

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:357-28-8 SDS

357-28-8Downstream Products

357-28-8Relevant articles and documents

(Z) -Trifluoromethyl-Trisubstituted Alkenes or Isoxazolines: Divergent Pathways from the Same Allene

Liu, Chaolun,Rowland, Casey A.,Tius, Marcus A.,Yap, Glenn P. A.

supporting information, p. 7208 - 7212 (2020/10/02)

Because of a charge-dipole interaction involving nonbonding electron pairs on fluorine, protonation of trifluoromethyl allenes leads to tri- or tetrasubstituted alkenes with high (Z)-selectivity. Treatment of the same allenes with catalytic Au(I) initiates a reaction cascade that produces isoxazolines in high yield.

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