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Cyclopentane, 1-fluoro-1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85982-46-3

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85982-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85982-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,8 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85982-46:
(7*8)+(6*5)+(5*9)+(4*8)+(3*2)+(2*4)+(1*6)=183
183 % 10 = 3
So 85982-46-3 is a valid CAS Registry Number.

85982-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-fluoro-1-methylcyclopentane

1.2 Other means of identification

Product number -
Other names -

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:85982-46-3 SDS

85982-46-3Downstream Products

85982-46-3Relevant academic research and scientific papers

Reaction of aminosulfur trifluorides with alcohols: inversion vs. retention

Shellhamer, Dale F.,Briggs, Alice A.,Miller, Becky M.,Prince, Jeanie M.,Scott, Dawn H.,Heasley, Victor L.

, p. 973 - 978 (2007/10/03)

Reaction of aminosulfur trifluorides with alcohols replaces the hydroxy group with fluorine.A study with the cyclic secondary alcohols trans-2-bromoindan-1-ol (3), trans-2-methylcyclopentanol (7), cis-2-methylcyclopentanol (8), trans-cyclopentanol (9), cis-cyclopentanol (10) and trans-2-fluorocyclopentanol (11) gave primarily inversion of configuration via an SN1-like pathway.The product stereochemistry and alkene formation in the reaction of aminosulfur trifluorides with cyclopentanols was similar to the products of solvolysis of cyclopentyl tosylates in methanol.The stereochemistry of the fluoro products was confirmed by independent synthesis or assigned by 1H and 19F NMR spectral data except for the deuteriated products 14 and 15 whose stereochemistry was assigned by their 2H NMR data.

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