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8-Oxomyristic acid, also known as 8-Oxotetradecanoic acid, is a naturally occurring organic compound that serves as an intermediate in the synthesis of various metabolites and has potential applications in different industries due to its unique chemical properties.

39747-88-1

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39747-88-1 Usage

Uses

Used in Chemical Synthesis:
8-Oxomyristic acid is used as an intermediate in the chemical synthesis process for producing 8-Hydroxytetradecanoic Acid (H954200), which is a metabolite of hydroxystearic acid. This application is significant as it contributes to the production of essential compounds utilized in various industrial and research applications.

Check Digit Verification of cas no

The CAS Registry Mumber 39747-88-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,4 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39747-88:
(7*3)+(6*9)+(5*7)+(4*4)+(3*7)+(2*8)+(1*8)=171
171 % 10 = 1
So 39747-88-1 is a valid CAS Registry Number.

39747-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-oxotetradecanoic acid

1.2 Other means of identification

Product number -
Other names 8CO-Myristic 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:39747-88-1 SDS

39747-88-1Relevant academic research and scientific papers

Synthesis of the Antifungal Agent Neoenactin A and Its N-Deshydroxy Derivative

Darwish, Ihab S.,Miller, Marvin J.

, p. 451 - 454 (2007/10/02)

The first total and unequivocal syntheses of neoenactin A (1, NE A) as well as its N-deshydroxy analog 2 are described.The two key steps in the syntheses were the oxidative cleavage of an appropriate olefin 8a to yield the desired keto acid 9 and the Mich

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