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16737-30-7

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16737-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16737-30-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,3 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16737-30:
(7*1)+(6*6)+(5*7)+(4*3)+(3*7)+(2*3)+(1*0)=117
117 % 10 = 7
So 16737-30-7 is a valid CAS Registry Number.

16737-30-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-methylcyclohexyl)acetate

1.2 Other means of identification

Product number -
Other names 1-Methyl-1-cyclohexyl acetate

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:16737-30-7 SDS

16737-30-7Relevant articles and documents

A Polymer-Bound 4-Aminopyridine: Synthesis and Reactivity

Menger, F. M.,McCann, D.J.

, p. 3928 - 3930 (1985)

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Cope et al.

, p. 1750,1751 (1960)

-

Isopropenyl acetate: A cheap and general acylating agent of alcohols under metal-free conditions

Temperini, Andrea,Minuti, Lucio,Morini, Tommaso,Rosati, Ornelio,Piazzolla, Francesca

, p. 4051 - 4053 (2017/09/27)

Functionalized primary, secondary and tertiary alcohols are efficiently acetylated by isopropenyl acetate and catalytic p-TsOH.

Iron(III) tosylate catalyzed acylation of alcohols, phenols, and aldehydes

Baldwin, Neil J.,Nord, Anna N.,O'Donnell, Brendan D.,Mohan, Ram S.

, p. 6946 - 6949 (2013/01/15)

Iron(III) p-toluenesulfonate (tosylate) is an efficient catalyst for acetylation of alcohols, phenols, and aldehydes. The acetylation of 1° and 2° alcohols, diols, and phenols proceeded smoothly with 2.0 mol % of catalyst. However, the reaction worked well with only a few 3° alcohols. The methodology was also applicable to the synthesis of a few benzoate esters but required the use of 5.0 mol % catalyst. Aldehydes could also be converted into the corresponding 1,1-diesters (acylals) under the reaction conditions. Iron(III) tosylate is an inexpensive, and easy to handle, commercially available catalyst.

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