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17173-14-7

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17173-14-7 Usage

General Description

7-hydroxy-octanoic acid is a compound that belongs to the class of hydroxy acids. It is also known as 7-HOA and is derived from the omega-3 fatty acid, docosahexaenoic acid. It is a natural metabolite found in the body and has been identified in various biological sources such as marine sponges and algae. 7-hydroxy-octanoic acid has been studied for its potential therapeutic properties, including anti-inflammatory and neuroprotective effects. It has also been investigated for its role in lipid metabolism and its potential as a biomarker for certain diseases. Overall, 7-hydroxy-octanoic acid is a promising compound with potential applications in the fields of medicine and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 17173-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,7 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17173-14:
(7*1)+(6*7)+(5*1)+(4*7)+(3*3)+(2*1)+(1*4)=97
97 % 10 = 7
So 17173-14-7 is a valid CAS Registry Number.
InChI:InChI=1/C33H36N4O6/c1-7-20-19(6)32(42)37-27(20)14-25-18(5)23(10-12-31(40)41)29(35-25)15-28-22(9-11-30(38)39)17(4)24(34-28)13-26-16(3)21(8-2)33(43)36-26/h7-8,13-14,34-35H,1-2,9-12,15H2,3-6H3,(H,36,43)(H,37,42)(H,38,39)(H,40,41)/b26-13+,27-14-

17173-14-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name <+/->-7-hydroxyoctanoic acid

1.2 Other means of identification

Product number -
Other names 7-HYDROXYOCTANOIC 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:17173-14-7 SDS

17173-14-7Relevant articles and documents

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Sugiyama,N. et al.

, p. 2713 - 2714 (1967)

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Stereospecific synthesis of 23-hydroxyundecylprodiginines and analogues and conversion to antimalarial premarineosins via a Rieske oxygenase catalyzed bicyclization

Kancharla, Papireddy,Lu, Wanli,Salem, Shaimaa M.,Kelly, Jane Xu,Reynolds, Kevin A.

, p. 11674 - 11689 (2014)

Facile and highly efficient synthetic routes for the synthesis of (S)- and (R)-23-hydroxyundecylprodiginines ((23S)-2, and (23R)-2), 23-ketoundecylprodiginine (3), and deuterium-labeled 23-hydroxyundecylprodiginine ([23-d]-2) have been developed. We demon

Characterization of CYP154F1 from Thermobifida fusca YX and Extension of Its Substrate Spectrum by Site-Directed Mutagenesis

Rühlmann, Ansgar,Groth, Georg,Urlacher, Vlada B.

, p. 478 - 485 (2018/02/06)

Previous studies on cytochrome P450 monooxygenases (CYP) from family 154 reported their substrate promiscuity and high activity. Hence, herein, the uncharacterized family member CYP154F1 is described. Screening of more than 100 organic compounds revealed

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