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13980-14-8

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13980-14-8 Usage

Definition

ChEBI: A long-chain fatty acid that is behenic (docosanoic) acid substituted at position 2 by a hydroxy group.

Check Digit Verification of cas no

The CAS Registry Mumber 13980-14-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,8 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13980-14:
(7*1)+(6*3)+(5*9)+(4*8)+(3*0)+(2*1)+(1*4)=108
108 % 10 = 8
So 13980-14-8 is a valid CAS Registry Number.
InChI:InChI=1/C22H44O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21(23)22(24)25/h21,23H,2-20H2,1H3,(H,24,25)

13980-14-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxybehenic acid

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-docosansaeure

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:13980-14-8 SDS

13980-14-8Relevant articles and documents

Role of the hydrophobic moiety of tumor promoters. Synthesis and activity of 2-alkylated benzolactams

Endo, Yasuyuki,Yokoyama, Akihiro

, p. 63 - 66 (2007/10/03)

The size and position of a hydrophobic moiety on a benzolactam skeleton, which reproduces the active conformation and biological activity of teleocidins, play an important role in the appearance of the activity. Compounds with alkyl groups of various sizes and shapes at the 2-position of benzolactam were synthesized. Structure-activity results indicate that a hydrophobic substituent at the C-2 position plays a critical role in the appearance of biological activities, as in the case of substitution at C-9.

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