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Δ2-cis-Hexadecenoic Acid, also known as 2-cis-hexadecenoic acid, is a naturally occurring unsaturated fatty acid with the chemical formula C16H30O2. It features a cis double bond between the 2nd and 3rd carbon atoms in a 16-carbon chain, which gives it unique chemical and physical properties. Δ2-cis-Hexadecenoic Acid is found in various plant oils and is known for its potential role in biological processes, such as cell membrane fluidity and signal transduction. Due to its specific structure, it may also have implications in the fields of nutrition and medicine, although further research is needed to fully understand its effects and applications.

2825-68-5

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2825-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2825-68-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2825-68:
(6*2)+(5*8)+(4*2)+(3*5)+(2*6)+(1*8)=95
95 % 10 = 5
So 2825-68-5 is a valid CAS Registry Number.

2825-68-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ?2-cis-Hexadecenoic Acid

1.2 Other means of identification

Product number -
Other names 14-Octadecenoic 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:2825-68-5 SDS

2825-68-5Downstream Products

2825-68-5Relevant academic research and scientific papers

Structure and absolute configuration of mycobactin J

Schwartz, Brett D.,De Voss, James J.

, p. 3653 - 3655 (2001)

Mycobactin J 1 is a commercially available siderophore isolated from Mycobacterium avium subsp. paratuberculosis. There are discrepancies between previous reports of its structure and none have addressed its absolute configuration. We report here the complete structure and stereochemistry of mycobactin J, along with methodology to enable the determination of the absolute configuration of other mycobactins on a small scale.

Total Synthesis of the Proposed Structure of Mycobactin J

Ghosh, Chiranjit,Pal, Sujit,Patel, Akanksha,Kapur, Manmohan

supporting information, p. 6511 - 6515 (2018/10/20)

The total synthesis of the proposed structure of mycobactin J (MJ), a metabolite of Mycobacterium tuberculosis, is presented. The highlights of the synthesis include a careful control of the Z-stereochemistry of the unsaturated long chain fatty acid, a biomimetic construction of the oxazoline building block and the carriage of an unprotected phenol throughout the synthesis.

Phosphonium Iodide in Organic Synthesis

Chatterjea, J. N.,Majee, R. N.,Mukherjee, S. N.

, p. 733 - 735 (2007/10/02)

Phosphonium iodide is found useful in the stereospecific conversion of some vicinal diols to olefins.Synthesis of cis-hexadec-9-enolide has been achieved.

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