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5939-87-7

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5939-87-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5939-87-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5939-87:
(6*5)+(5*9)+(4*3)+(3*9)+(2*8)+(1*7)=137
137 % 10 = 7
So 5939-87-7 is a valid CAS Registry Number.

5939-87-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4,4-trimethyl-1-cyclohexene)carbaldehyde

1.2 Other means of identification

Product number -
Other names β-cyclolavandulal

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:5939-87-7 SDS

5939-87-7Relevant articles and documents

Method for producing [beta]-cyclolavandulal and derivative of same

-

Paragraph 0110; 0111; 0112; 0113; 0114; 0115; 0116-0118, (2016/12/22)

A given compound is synthesized simply, efficiently, and selectively. Specifically, provided are a method for producing (2,4,4-trimethyl-1-cyclohexene)carbaldehyde including at least a step for obtaining a 2,4,4-trimethyl-2-cyclohexenylidene methyl ether compound (2) by reacting the carbonyl groups of 2,4,4-trimethyl-2-cyclohexenone (1) and a step for obtaining (2,4,4-trimethyl-1-cyclohexene)carbaldehyde (3) by hydrolyzing (2), a method for producing (2,4,4-trimethyl-1-cyclohexene)methanol including at least a step for obtaining (2,4,4-trimethyl-1-cyclohexene)methanol (4) by reducing (3), and a method for producing a (2,4,4-trimethyl-1-cyclohexenyl)methyl ester compound including at least a step for obtaining a (2,4,4-trimethyl-1-cyclohexenyl)methyl ester compound (5) by esterifying (4).

An efficient synthetic method for β-cyclolavandulal and its corresponding alcohol

Oda, Mitsunori,Isobe, Atsushi,Hayashi, Masashi,Miyatake, Ryuta,Shimao, Ichiro,Kuroda, Shigeyasu

, p. 438 - 440 (2007/10/03)

3,3-Dimethylcyclohexanone (5) was efficiently converted to methyl β-cyclolavandulate (6) in 74% yield in three steps, one of which included the preparation of β-methyl α,β-unsaturated esters by coupling lithium dimethylcuprate with enol phosphates of β-ox

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