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

60380-79-2

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60380-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60380-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,8 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60380-79:
(7*6)+(6*0)+(5*3)+(4*8)+(3*0)+(2*7)+(1*9)=112
112 % 10 = 2
So 60380-79-2 is a valid CAS Registry Number.

60380-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-4-tert-Butyl-1-(hydroxymethyl)-1-cyclohexanol

1.2 Other means of identification

Product number -
Other names 4-tert-Butyl-1-hydroxymethyl-cyclohexanol

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:60380-79-2 SDS

60380-79-2Downstream Products

60380-79-2Relevant academic research and scientific papers

Torsional, rotor, and electronic effects in 4-tert-butylmethylenecyclohexane epoxidations and osmylations

Vedejs,Dent III,Kendall,Oliver

, p. 3556 - 3567 (2007/10/03)

The axial epoxidation preference for 2-substituted 4-tert-butylmethylenecyclohexanes is attributed to a combination of small effects, including existing bond torsion and rotor effects. Contributions from developing bond torsion are smaller and may be negl

Practical hydroxymethylation of aldehydes and ketones via pinacol cross-coupling reactions with paraformaldehyde

Park, Jeonghan,Pedersen, Steven F.

, p. 2069 - 2080 (2007/10/02)

A general and practical method for the direct hydroxymethylation of aldehydes and ketones via pinacol cross-coupling with paraformaldehyde is described. The reaction is promoted by vanadium(II) ions which are conveniently generated from the reduction of VCl3(THF)3 with zinc dust. Excellent yields of terminal diols are obtained and stereoselective coupling is observed with some chiral aldehydes and ketones.

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