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3589-73-9

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3589-73-9 Usage

Description

A carboline alkaloid, this base occurs in the stems and leaves of Virola cuspidata. The structure has been shown to be 3:4-dihydro-6-methoxy-l-methyl-iJ-carboline from spectroscopic evidence.

Uses

Different sources of media describe the Uses of 3589-73-9 differently. You can refer to the following data:
1. 6-Methoxyharmalan is useful in the treatment of autophagy-associated disorders
2. ? ;Reactant for preparation of TRPV1-dependent vasodilator1

References

Cassady et al., Lioydia, 34, 161 (1971)

Check Digit Verification of cas no

The CAS Registry Mumber 3589-73-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,8 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3589-73:
(6*3)+(5*5)+(4*8)+(3*9)+(2*7)+(1*3)=119
119 % 10 = 9
So 3589-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H14N2O/c1-8-13-10(5-6-14-8)11-7-9(16-2)3-4-12(11)15-13/h3-4,7,15H,5-6H2,1-2H3

3589-73-9SDS

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 6-methoxy-1-methyl-3,4-dihydro-2H-pyrido[3,4-b]indole

1.2 Other means of identification

Product number -
Other names 2-methoxyharmalane

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:3589-73-9 SDS

3589-73-9Relevant articles and documents

1,1-disubstituted-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indolecarboxylic acid esters and ketones. The base catalyzed transformation of 1-(2',3',4',9'-tetrahydrospiro[cyclohexane-1,1'-[1H]pyrido[3,4-b]indol]- 2-yl)alkanones into 2-(4,9-dihydro-3H-pyrido[3,4-b]indol-1-yl)-1-alkylcyclohexanols

Bobowski,Shavel Jr.

, p. 1679 - 1688 (2007/10/02)

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