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20785-90-4

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20785-90-4 Usage

Chemical class

beta-carboline alkaloids

Derivative

1H-beta-carboline-1-one

Methyl group positions

2 and 9

Potential pharmacological activities

Yes

Neuropharmacological properties

Yes, affecting neurotransmitter systems

Therapeutic applications

Potential use in treating Parkinson's disease and dementia

Ongoing research

In the fields of medicinal chemistry and neuropharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 20785-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,8 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20785-90:
(7*2)+(6*0)+(5*7)+(4*8)+(3*5)+(2*9)+(1*0)=114
114 % 10 = 4
So 20785-90-4 is a valid CAS Registry Number.

20785-90-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,9-dimethyl-3,4-dihydropyrido[3,4-b]indol-1-one

1.2 Other means of identification

Product number -
Other names -

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:20785-90-4 SDS

20785-90-4Relevant articles and documents

-

Gupta,Spenser

, p. 2049,2055 (1962)

-

Method for synthesizing tetrahydro beta-carboline-1-one compound through palladium catalysis

-

Paragraph 0064; 0065; 0066; 0067, (2017/10/06)

The invention discloses a method for synthesizing a tetrahydro beta-carboline-1-one compound through palladium catalysis. According to the method, carbonic oxide is used as a carbonyl source; the carbonic oxide and a tryptamine type compound react at ordinary pressure for efficiently preparing the tetrahydro beta-carboline-1-one compound. The method has the advantages that the tetrahydro beta-carboline-1-one compound with great application prospects is effectively prepared by using the carbonic oxide at the ordinary pressure as the carbonyl source and using bivalent metal palladium as a catalyst. From the angle of production and economy, through being compared with high-pressure reaction, the method has the advantages that the reaction cost is greatly reduced through carbonic oxide gas at normal temperature, and the reaction operability is improved.

The Reactions of Some Tetrahydro-β-Carbolines, of Hexahydroazepinoindoles, and of Tetrahydrocarbazolones with Arenesulphonyl Azides

Bailey, A. Sydney,Vandrevala, Marazban H.

, p. 1512 - 1515 (2007/10/02)

2,9-Dimethyl-1,2,3,4-tetrahydro-1-oxo-β-carboline and 2,9-dimethyl-1,2,3,4-tetrahydro-β-carboline react with arenesulphonyl azides forming indoline-3-spiropyrrolidines; 2,10-dimethyl-3,4,5,10-tetrahydroazepinoindol-1(2H)-0ne and 2,10-dimethyl-1,2,3

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