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6-Octenoic acid, 3-hydroxy-7-methyl-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93041-01-1

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93041-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93041-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,0,4 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 93041-01:
(7*9)+(6*3)+(5*0)+(4*4)+(3*1)+(2*0)+(1*1)=101
101 % 10 = 1
So 93041-01-1 is a valid CAS Registry Number.

93041-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R)-7-methyl-3-hydroxyoct-6-enoic acid

1.2 Other means of identification

Product number -
Other names (R)-3-hydroxy-7-methyl-6-octenoic 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:93041-01-1 SDS

93041-01-1Relevant academic research and scientific papers

CeCl3·7H2O-Nal Catalyzed Hydrooxacyclization of Unsaturated 3-Hydroxy Esters

Marotta, Emanuela,Foresti, Elisabetta,Marcelli, Tommaso,Peri, Francesca,Righi, Paolo,Scardovi, Noemi,Rosini, Goffredo

, p. 4451 - 4453 (2002)

(Matrix Presented) Cerium(III) chloride heptahydrate and sodium iodide in boiling acetonitrile promote cyclization of 3-hydroxyalkenoic acids esters giving 5-substituted tetrahydrofuranacetic acid esters and 6-substituted tetrahydropyranacetic acid esters

A USEFUL METHOD FOR PREPARING OPTICALLY ACTIVE SECONDARY ALCOHOLS: A SHORT ENANTIOSPECIFIC SYNTHESIS OF (R)- AND (S)-SULCATOL

Afonso, Carlos M.,Barros, M. Teresa,Godinho, Licio,Maycock, Christopher D.

, p. 2707 - 2708 (1989)

The epimeric 2-(1-Hydroxyethyl)-5-methyl-4-hexanoic acids have been prepared by bakers yeast reduction of the corresponding oxo compound or by alkylation of an optically pure 3-hydroxybutanoate.Radical chain decarboxylation afforded the antipodes of sulca

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