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68922-15-6

3-[(acetoxy)methyl]nonan-1-oic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68922-15-6

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68922-15-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68922-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,9,2 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68922-15:
(7*6)+(6*8)+(5*9)+(4*2)+(3*2)+(2*1)+(1*5)=156
156 % 10 = 6
So 68922-15-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O4/c1-3-4-5-6-7-11(8-12(14)15)9-16-10(2)13/h11H,3-9H2,1-2H3,(H,14,15)

68922-15-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(acetyloxymethyl)nonanoic acid

1.2 Other means of identification

Product number -
Other names 3-Acetoxymethylnonanoic acid

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:68922-15-6 SDS

68922-15-6Downstream Products

68922-15-6Relevant articles and documents

Synthesis and olfactory evaluation of optically active β-alkyl substituted γ-lactones and whiskey lactone analogues

Kato, Daiki,Kawasaki, Masashi,Morita, Yuko,Okada, Takuya,Tanaka, Yasuo,Toyooka, Naoki

supporting information, (2020/02/22)

Optically active β-alkyl substituted γ-lactones and whiskey lactone analogues were synthesized, and the odor properties were evaluated. During the preparation of the chiral intermediates, we found good reaction conditions for the highly enantioselective esterification of 3-arylmethyl-2-methyl-1-propanols to kinetically resolve them. The results of the olfactory evaluations of the synthesized lactones revealed that the alkyl groups on the γ-lactone rings played an important role for the odor profiles.

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