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1268720-66-6

7(S)-Maresin 1 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1268720-66-6

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1268720-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268720-66-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,7,2 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1268720-66:
(9*1)+(8*2)+(7*6)+(6*8)+(5*7)+(4*2)+(3*0)+(2*6)+(1*6)=176
176 % 10 = 6
So 1268720-66-6 is a valid CAS Registry Number.

1268720-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (7S,14R)-7,14-dihydroxydocosa-4,8,10,12,16,19-hexaenoic acid

1.2 Other means of identification

Product number -
Other names 7S,14S-dihydroxydocosa-4Z,8E,10E,12Z,16Z,19Z-hexaenoic 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:1268720-66-6 SDS

1268720-66-6Downstream Products

1268720-66-6Relevant articles and documents

Total synthesis and bioactivities of two proposed structures of maresin

Sasaki, Kenji,Urabe, Daisuke,Arai, Hiroyuki,Arita, Makoto,Inoue, Masayuki

, p. 534 - 543 (2011/10/12)

Maresin is a potent anti-inflammatory lipid mediator derived from docosahexaenoic acid (DHA). A highly convergent total synthesis of two proposed structures of C7-epimeric maresins from the four known fragments was achieved in 17 steps. The three key coupling reactions were the BF3-mediated alkyne attack on the epoxide, chiral titanium complex-promoted enantioselective alkyne addition to the aldehyde, and a Julia-Kocienski olefination. The two synthesized diastereomers were found to be comparably active in blocking neutrophil infiltration in the acute peritonitis model. Copyright

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