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1-Nonacosanol, 3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144751-00-8

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144751-00-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144751-00-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,7,5 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 144751-00:
(8*1)+(7*4)+(6*4)+(5*7)+(4*5)+(3*1)+(2*0)+(1*0)=118
118 % 10 = 8
So 144751-00-8 is a valid CAS Registry Number.

144751-00-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylnonacosan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Nonacosanol,3-methyl

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:144751-00-8 SDS

144751-00-8Upstream product

144751-00-8Downstream Products

144751-00-8Relevant academic research and scientific papers

Synthesis of racemic and each enantiomer of 3-methylnonacosanol, a new plant growth regulator from Lowsonia inermis

Kulkarni, Bheemashankar A.,Sankaranarayanan, Sivaraman,Subbaraman, Ayalur S.,Chattopadhyay, Subrata

, p. 1571 - 1577 (2007/10/03)

An efficient synthesis of the title compound I in racemic and enantiomeric forms has been developed starting from 10-undecenoic acid. For the enantiomeric synthesis, a lipase catalyzed acylation strategy was employed to prepare the required methyl branched chiron which was subsequently derivatized to give the enantiomers of I. The plant growth regulatory (PGR) assay of I, carried out with hypocotyl cuttings of French beans (Phaseolus vulgaris L.) in Steinberg's nutrient medium revealed appreciable activity at a concentration of 2.5 ppm. The PGR activities of the compound both in racemic and enantiomeric forms were better than 1- triacontanol, the enantiomer, (S)-I being the best test candidate.

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