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3-methyl-5-propylcyclohexan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67662-98-0

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67662-98-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67662-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,6 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67662-98:
(7*6)+(6*7)+(5*6)+(4*6)+(3*2)+(2*9)+(1*8)=170
170 % 10 = 0
So 67662-98-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-3-4-9-5-8(2)6-10(11)7-9/h8-9H,3-7H2,1-2H3

67662-98-0SDS

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 3-methyl-5-propylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names Cyclohexanone,3-methyl-5-propyl

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:67662-98-0 SDS

67662-98-0Downstream Products

67662-98-0Relevant academic research and scientific papers

STEREOCHEMICAL ASSIGMENT BY MASS SPECTROMETRY. DOUBLE BOND GEOMETRICAL ISOMERS OF 3,5-DIALKYLCYCLOHEXYLIDENE ACETIC ACID ESTERS AND 3-ALKYL-2-ALKENOATES

Merksammer, Israel,Mandelbaum, Asher

, p. 775 - 780 (2007/10/02)

Mass spectrometry is best physical method for the configurational assignment of E- and Z-3,5-dialkylcyclohexylidene acetic acid esters 1 and E- and Z-3-alkyl-2-alkenoates 2.The homoallylic cleavage resulting in the loss of the C-3 and C-5 alkyl groups from 1 and of the two δ-alkyls from 2 is a stereospecific process: the loss of the group which is adjacent to the carbonyl is significantly preferred.The stereospecifity of this fragmentation is interpreted in terms of a hidden hydrogen transfer preceding the carbon-carbon bond cleavage.

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