Welcome to LookChem.com Sign In|Join Free
  • or
2-methyleicosanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22890-19-3

Post Buying Request

22890-19-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

22890-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22890-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,9 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22890-19:
(7*2)+(6*2)+(5*8)+(4*9)+(3*0)+(2*1)+(1*9)=113
113 % 10 = 3
So 22890-19-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H42O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(2)21(22)23/h20H,3-19H2,1-2H3,(H,22,23)

22890-19-3SDS

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 2-Methylicosanoic acid

1.2 Other means of identification

Product number -
Other names a-Methylarachidic 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:22890-19-3 SDS

22890-19-3Relevant academic research and scientific papers

Sulfoglycolipid antigens, their process of preparation, and their use against tuberculosis

-

, (2008/12/07)

The present invention relates to compounds of the following general formula: their process of preparation and their use in the treatment or the prophylaxis of tuberculosis.

Synthesis of methyl (Z)-tetracos-5-enoate and both enantiomers of ethyl (E)-6-methyltetracos-4-enoate: Possible intermediates in the biosynthesis of mycolic acids in mycobacteria

Besra, Gurdyal S.,Minnikin, David E.,Wheeler, Paul R.,Ratledge, Colin

, p. 23 - 34 (2007/10/02)

The high molecular weight 2-alkyl-3-hydroxy mycolic acids are key structural components of the cell envelope of pathogenic mycobacteria, such as Mycobacterium tuberculosis. A prime target for drug action would be the initial stages where the biosynthetic pathways diverge from those of ordinary fatty acids. It has been postulated that the pathway for the α-mycolates, without oxygen functions in addition to the hydroxy-acid unit, appears to diverge from (Z)-tetracos-5-enoic acid. The biosynthesis of oxygenated mycolic acids is considered to possibly diverge from (E)-6-(R)-methyltetracos-4-enoic and (E)-6-(S)-methyltetracos-4-enoic acids. This communication describes the synthesis of esters of these acids in order to test their potential role in the biosynthesis of mycolic acids.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 22890-19-3