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4-hydroxy-3,6,10-trimethylundec-9-en-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68141-16-2

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68141-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68141-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,4 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 68141-16:
(7*6)+(6*8)+(5*1)+(4*4)+(3*1)+(2*1)+(1*6)=122
122 % 10 = 2
So 68141-16-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O2/c1-10(2)7-6-8-11(3)9-14(16)12(4)13(5)15/h7,11-12,14,16H,6,8-9H2,1-5H3

68141-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-3,6,10-trimethylundec-9-en-2-one

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-3,6,10-trimethyl-9-undecen-2-one

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:68141-16-2 SDS

68141-16-2Relevant academic research and scientific papers

Synthesis and olfactory evaluation of bulky moiety-modified analogues to the sandalwood odorant polysantol

Chapado, Laura,Linares-Palomino, Pablo J.,Badia, Concepcion,Salido, Sofia,Nogueras, Manuel,Sanchez, Adolfo,Altarejos, Joaquin

experimental part, p. 2780 - 2800 (2010/03/24)

Five new bulky moiety-modified analogues of the sandalwood odorant Polysantol have been synthesized by aldol condensation of appropriate aldehydes with butanone, deconjugative α-methylation of the resulting α,β-unsaturated ketones, and reduction of the co

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