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31375-17-4

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  • BEST PRICE/ 1-p-menth-6-en-2-yl-1-propanon Manufacturer CAS NO.31375-17-4

    Cas No: 31375-17-4

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31375-17-4 Usage

Safety Profile

A skin irritant. A flammable liquid. When heated to decomposition it emits acrid smoke and irritating fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 31375-17-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,3,7 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 31375-17:
(7*3)+(6*1)+(5*3)+(4*7)+(3*5)+(2*1)+(1*7)=94
94 % 10 = 4
So 31375-17-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H22O/c1-5-13(14)12-8-11(9(2)3)7-6-10(12)4/h6,9,11-12H,5,7-8H2,1-4H3

31375-17-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methyl-5-propan-2-ylcyclohex-2-en-1-yl)propan-1-one

1.2 Other means of identification

Product number -
Other names 1-PROPANONE,1-p-MENTH-6-EN-2-YL

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:31375-17-4 SDS

31375-17-4Downstream Products

31375-17-4Relevant articles and documents

ADDITION RADICALAIRE DU PROPANAL A DIVERS ALCENES ET CYCLENES : ASPECTS STERIQUES ET POLAIRES

Tabbaa, I.,Cazaux, M.,Lalande, R.

, p. 1011 - 1018 (2007/10/02)

Free radical addition of propanal to double bonds, initiated by benzoyl peroxide, mainly leads to two adducts, an aldehyde and a ketone, when the double bond has a methylene group ; these results are explained in terms of polar effects in the free radical transfert reactions.When the double bond has no methylene group, only the ketonic adduct is obtained ; the steric effects in the free radical addition step explain these results.

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