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28393-06-8

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28393-06-8 Usage

General Description

10,12-Heptadecadiynoic acid is a long-chain carboxylic acid with a 17-carbon backbone and two terminal alkyne groups. It is classified as a fatty acid due to its structure, and it is often used in research and pharmaceutical applications. Heptadecadiynoic acid has been studied for its potential anti-inflammatory and anti-microbial properties, as well as its ability to inhibit the growth of cancer cells. In addition, it has been investigated for its potential use in electronic and optical devices, due to its unique electronic and optical properties. Overall, 10,12-heptadecadiynoic acid is a versatile chemical with potential applications in a wide range of fields.

Check Digit Verification of cas no

The CAS Registry Mumber 28393-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,9 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28393-06:
(7*2)+(6*8)+(5*3)+(4*9)+(3*3)+(2*0)+(1*6)=128
128 % 10 = 8
So 28393-06-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H26O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(18)19/h2-4,9-16H2,1H3,(H,18,19)

28393-06-8SDS

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 heptadeca-10,12-diynoic acid

1.2 Other means of identification

Product number -
Other names Heptadeca-10,12-diin-1-saeure

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:28393-06-8 SDS

28393-06-8Downstream Products

28393-06-8Relevant articles and documents

Synthesis and Nuclear Magnetic Resonance Studies on a Series of Synthesis Long-chain Tellurophene Fatty Esters

Jie, Marcel S. F. Lie Ken,Chau, Sherman H.

, p. 2642 - 2657 (2007/10/03)

The synthesis and the results of the 1H and 13C NMR spectroscopic analyses of thirteen 2,5-disubstituted tellurophene fatty esters, containing substituents of different chain lengths, and of a monosubstituted tellurophene ester are repported.The tellurophene esters are obtained by cyclization of the corresponding conjugated intermediates with Na2Te in the presence of AgOAc in methanol.The tellurophene moiety in the alkyl chain induces a deshielding effect on the protons of the adjacent methylene prtons.The shift parameters of the tellurophene moiety on the shifts of the adjacent methylene carbon atoms are also determined.

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