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Benzoic acid,4-fluoro-,2-(3,4,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indol-2(1H)-yl)ethylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77293-99-3

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77293-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77293-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,9 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77293-99:
(7*7)+(6*7)+(5*2)+(4*9)+(3*3)+(2*9)+(1*9)=173
173 % 10 = 3
So 77293-99-3 is a valid CAS Registry Number.

77293-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name BRN 4585386

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:77293-99-3 SDS

77293-99-3Downstream Products

77293-99-3Relevant academic research and scientific papers

Agents Acting on CNS: Part XXX - Synthesis of 2-Substituted 1,2,3,4,6,7,12,12a-Octahydropyrazinopyrido-indoles

Dhaon, Madhup K.,Kumar, Naresh,Agarwal, Shiv K.,Saxena, Anil K.,Jain, Padam C.,Anand, Nitya

, p. 882 - 885 (2007/10/02)

A number of 2-substituted pyrazinopyridoindoles (3,6-12) have been prepared by the condensation of 1,2,3,4,6,7,12,12a-octahydropyrazinopyridoindole (1) with appropriate halogen compounds.Treatment of 1 with ethylene oxide gives 4 which on condensation with p-fluorobenzoyl chloride yields 5.The corresponding 2-γ-(p-fluorobenzoyl)propyl-6-oxo-octahydropyrazinopyridoindole (14) is prepared by the oxidation of 1 with mercuric acetate followed by condensation of the resulting 6-oxo derivative (13) with γ-chloro-p-fluorobutyrophenone. 1-Oxo-2-substituted-pyrazinopyridoindoles (16-18) are prepared by the reaction of ethylene oxide on methyl 1,2,3,4-tetrahydropyridoindole-3-carboxylate followed by condensation of the resulting oxazino derivative (15) with amines.These compounds show tranquillizing, anti-inflammatory and diuretic activities.

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