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23544-42-5

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23544-42-5 Usage

General Description

The chemical compound "(3aS,6R,7aS)-3a-(3,4-dimethoxyphenyl)-1-methyloctahydro-1H-indol-6-ol" is a complex organic molecule with a molecular formula C18H31NO3. It consists of a bicyclic structure with a 1H-indol-6-ol core, a dimethoxyphenyl group, and a methyl substituent. (3aS,6R,7aS)-3a-(3,4-dimethoxyphenyl)-1-methyloctahydro-1H-indol-6-ol may have potential applications in pharmaceuticals, particularly in the development of new drugs targeting neurological disorders or in the field of medicinal chemistry due to its unique structure and potential biological activities. Further research is needed to fully understand and utilize the properties and applications of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 23544-42-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,4 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23544-42:
(7*2)+(6*3)+(5*5)+(4*4)+(3*4)+(2*4)+(1*2)=95
95 % 10 = 5
So 23544-42-5 is a valid CAS Registry Number.

23544-42-5SDS

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 (3aS,6R,7aS)-3a-(3,4-dimethoxyphenyl)-1-methyl-3,4,5,6,7,7a-hexahydro-2H-indol-6-ol

1.2 Other means of identification

Product number -
Other names Mesembrinol

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:23544-42-5 SDS

23544-42-5Relevant articles and documents

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Bodendorf,Krieger

, p. 441,445 (1957)

-

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Popelak et al.

, p. 156 (1960)

-

Chiral synthesis of (-)-mesembranol starting from D-glucose

Chida,Sugihara,Ogawa

, p. 901 - 902 (2007/10/02)

The chiral synthesis of the Sceletium alkaloid, (-)-mesembranol 1 is described; the cyclohexane ring in 1 is prepared in an optically active form from D-glucose using Ferrier's carbocyclisation reaction and the perhydroindole skeleton is effectively constructed by an intramolecular aminomercuration reaction.

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