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2-Ethenyl-3-phenyl-2-(trifluoromethyl)oxirane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

191591-48-7

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191591-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 191591-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,5,9 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 191591-48:
(8*1)+(7*9)+(6*1)+(5*5)+(4*9)+(3*1)+(2*4)+(1*8)=157
157 % 10 = 7
So 191591-48-7 is a valid CAS Registry Number.

191591-48-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethenyl-3-phenyl-2-(trifluoromethyl)oxirane

1.2 Other means of identification

Product number -
Other names PC6261

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:191591-48-7 SDS

191591-48-7Downstream Products

191591-48-7Relevant academic research and scientific papers

Fluorinated vinyl oxiranes

-

, (2008/06/13)

A compound having the formula: STR1 wherein: R is fluorine, hydrogen, an unsubstituted or substituted aliphatic or unsubstituted or substituted aromatic radical; R1 is an unsubstituted or substituted aliphatic radical, or unsubstituted or substituted aromatic radical; and R2 is hydrogen, an unsubstituted or substituted aliphatic radical, or unsubstituted or substituted aromatic radical.

1,3-Dichloro-4,4,4-trifluorobut-2-ene as a 4-carbon building block containing a trifluoromethyl group

Van Der Puy, Michael

, p. 187 - 191 (2007/10/03)

The preparation, isomerization, and utility of CF3CCl=CHCH2Cl as a 4-carbon reagent for the incorporation of a trifluoromethyl group is described. The regiochemistry observed for charged intermediates derived from CF3CCl=CHCH2Cl was consistent with MNDO calculated partial charges at C-1 and C-3. The anion-stabilizing and cation-destabilizing effects of the trifluoromethyl group were dominant.

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