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6-Octadecynoic acid methyl ester is a chemical compound with the molecular formula C19H34O2. It is an organic ester derived from 6-octadecynoic acid, which is an unsaturated fatty acid containing an alkyne group. 6-Octadecynoic acid methyl ester is characterized by a long hydrocarbon chain with 18 carbon atoms and a triple bond at the 6th position, with a carboxyl group at the end. The esterification of the carboxyl group with methanol results in the formation of a methyl ester group, making it a valuable intermediate in the synthesis of various chemicals, such as surfactants, lubricants, and pharmaceuticals. Its unique structure with a triple bond and a long hydrocarbon chain contributes to its specific properties and applications in various industries.

2777-64-2

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2777-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2777-64-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,7 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2777-64:
(6*2)+(5*7)+(4*7)+(3*7)+(2*6)+(1*4)=112
112 % 10 = 2
So 2777-64-2 is a valid CAS Registry Number.

2777-64-2SDS

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 methyl octadec-6-ynoate

1.2 Other means of identification

Product number -
Other names octadec-6-ynoic acid methyl ester

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:2777-64-2 SDS

2777-64-2Downstream Products

2777-64-2Relevant academic research and scientific papers

Acetylenic acids inhibiting azole-resistant Candida albicans from Pentagonia gigantifolia

Li, Xing-Cong,Jacob, Melissa R.,ElSohly, Hala N.,Nagle, Dale G.,Smillie, Troy J.,Walker, Larry A.,Clark, Alice M.

, p. 1132 - 1135 (2003)

Antifungal bioassay-guided isolation of the ethanol extract of the roots of Pentagonia gigantifolia yielded 6-octadecynoic acid (1) and the new 6-nonadecynoic acid (2). Compounds 1 and 2 inhibited the growth of fluconazole-susceptible and -resistant Candida albicans strains. Their antifungal potencies were comparable to those of amphotericin B and fluconazole. Of particular significance is the low cytotoxicity and specific activity of 1 and 2 against C. albicans.

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