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Cyclohexane, 1-(1,1-dimethylethyl)-1-fluoro-4-methyl-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90304-29-3

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90304-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90304-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,0 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90304-29:
(7*9)+(6*0)+(5*3)+(4*0)+(3*4)+(2*2)+(1*9)=103
103 % 10 = 3
So 90304-29-3 is a valid CAS Registry Number.

90304-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-t-butyl-1-fluoro-4-methylcyclohexane

1.2 Other means of identification

Product number -
Other names 1-tert-Butyl-1-fluoro-4-methyl-cyclohexane

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:90304-29-3 SDS

90304-29-3Downstream Products

90304-29-3Relevant academic research and scientific papers

ACTIVATION OF TERTIARY PARAFFINS BY ELEMENTAL FLUORINE

Gal, Chava,Rozen, Shlomo

, p. 449 - 452 (1984)

Elemental fluorine was found to substitute, in a regio and stereospecific way, tertiary unactivated hydrogens in alkanes - the most unreactive family of organic compounds.

Activating Unreactive Sites of Organic Molecules Using Elemental Fluorine

Rozen, Shlomo,Gal, Chava

, p. 2769 - 2779 (2007/10/02)

Electrophilic substitution reactions on saturated carbons are extremely rare.Elemental fluorine, however, uses this pathway to replace tertiary unactivated hydrogens with great regio- and stereoselectivity, resulting in a full retention of configuration.I

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