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5523-37-5

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5523-37-5 Usage

General Description

The chemical compound (15S,16E)-16,17,20,21-Tetradehydro-16-formyl-18,19-secoyohimban-19-oic acid methyl ester is a complex organic molecule with a long and specific chemical structure. It contains a formyl group and is a derivative of yohimbine, a natural alkaloid found in the bark of the yohimbe tree. (15S,16E)-16,17,20,21-Tetradehydro-16-formyl-18,19-secoyohimban-19-oic acid methyl ester is a methyl ester, which means it is an ester of methanol and the carboxylic acid group of the molecule. It is likely to have pharmaceutical or biological activity due to its complex structure and association with yohimbine, which is known for its potential use in the treatment of erectile dysfunction and as a stimulant. Further research and analysis are needed to fully understand the properties and potential uses of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 5523-37-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,2 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5523-37:
(6*5)+(5*5)+(4*2)+(3*3)+(2*3)+(1*7)=85
85 % 10 = 5
So 5523-37-5 is a valid CAS Registry Number.
InChI:InChI=1/C21H22N2O3/c1-3-13(12-24)16-10-19-20-15(14-6-4-5-7-18(14)22-20)8-9-23(19)11-17(16)21(25)26-2/h3-7,11-12,16,19,22H,8-10H2,1-2H3/b13-3-/t16-,19?/m0/s1

5523-37-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2S)-2-[(E)-1-oxobut-2-en-2-yl]-1,2,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine-3-carboxylate

1.2 Other means of identification

Product number -
Other names 18,19-Secoyohimban-19-oic acid,16,17,20,21-tetradehydro-16-formyl-,methyl ester,(15beta,16E)

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:5523-37-5 SDS

5523-37-5Relevant articles and documents

Bacterial biotransformation of 3α(S)-strictosidine to the monoterpenoid indole alkaloid vallesiachotamine

Shen, Zhengwu,Eisenreich, Wolfgang,Kutchan, Toni M.

, p. 293 - 296 (2007/10/03)

3α(S)-Strictosidine produced by heterologously expressed strictosidme synthase from Rauwolfia serpentina was used in biotransformation experiments with a series of 22 bacterial strains.All strains tested were found to deglucosylate and rearrange the alkaloid to vallesiachotamine, thereby providing an example of how gene technology and microbial biotransformation can be combined for the biotechnological production of alkaloidal natural products. - Keywords: Rauwolfia serpentina, Spodoptera frugiperda, baculovirus, strictosidine synthase, vallesiachotamine.

Addition von chiralen Nucleophilen an Pyridiniumverbindungen; Totalsynthese von (-)-Isovallesiachotamin und (+)-Vallesiachotamin

Amann, Robert,Spitzner, Dietrich

, p. 1373 - 1374 (2007/10/02)

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Totalsynthese des Indolalkaloids Vallesiachotamin

Spitzner, Dietrich,Wenkert, Ernest

, p. 972 - 975 (2007/10/02)

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