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101417-71-4

3-HYDROXY-3-(PENTAFLUOROETHYL)CYCLOHEXENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

101417-71-4

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101417-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101417-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,4,1 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 101417-71:
(8*1)+(7*0)+(6*1)+(5*4)+(4*1)+(3*7)+(2*7)+(1*1)=74
74 % 10 = 4
So 101417-71-4 is a valid CAS Registry Number.

101417-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1,1,2,2,2-pentafluoroethyl)cyclohex-2-en-1-ol

1.2 Other means of identification

Product number -
Other names 2-Cyclohexen-1-ol,1-(pentafluoroethyl)

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:101417-71-4 SDS

101417-71-4Downstream Products

101417-71-4Relevant articles and documents

Nucleophilic Addition of the Pentafluoroethyl Group to Aldehydes, Ketones, and Esters

Gassman, Paul G.,O'Reilly, Neil J.

, p. 2481 - 2490 (2007/10/02)

Pentafluoroethyl iodide reacts with methyllithium at -78 deg C to produce (pentafluoroethyl)lithium.This halogen-metal exchange reaction can be carried out in the presence of aldehydes, ketones, and esters with no observable addition of methyllithium to t

PENTAFLUOROETHYLLITHIUM. GENERATION AND USE IN SYNTHESIS

Gassman, Paul G.,O'Reilly, Neil J.

, p. 5243 - 5246 (2007/10/02)

Pentafluoroethyl iodide undergoes a rapid exchange reaction with methyllithium at -78 deg C in the presence of ketones to produce pentafluoroethyl-substituted tertiary carbinols in high yield.

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