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104915-39-1

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104915-39-1 Usage

Chemical structure

Contains both an amino group and a carbonitrile group

Use

Often used in research and pharmaceutical development

Application

Used in the synthesis of new drugs and potential pharmaceutical agents

Value

Valuable building block for creating new compounds with therapeutic applications

Potential use

Medicinal chemistry, specifically in the development of new drugs for various medical conditions

Check Digit Verification of cas no

The CAS Registry Mumber 104915-39-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,9,1 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104915-39:
(8*1)+(7*0)+(6*4)+(5*9)+(4*1)+(3*5)+(2*3)+(1*9)=111
111 % 10 = 1
So 104915-39-1 is a valid CAS Registry Number.

104915-39-1SDS

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 (R,S)-2-amino-4,5,6,7-tetrahydro-1-(1-phenylethyl)-1H-indole-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-Amino-1-(1-phenyl-ethyl)-4,5,6,7-tetrahydro-1H-indole-3-carbonitrile

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:104915-39-1 SDS

104915-39-1Relevant articles and documents

Synthesis of Substituted Indoles and Pyrimidoindoles by Dehydrogebation of Tetrahydroindoles and Tetrahydropyrimidoindoles

Eger, Kurt,Lanzner, Wolfgang,Rothenhaeusler, Klaus

, p. 465 - 470 (2007/10/02)

The synthesis of N1-substituted 2-amino-4,5,6,7-tetrahydroindole-3-carbonitriles 2 and 5,6,7,8-tetrahydropyrimidoindoles 3-5 and their subsequent dehydrogenation to the corresponding 2-aminoindole-3-carbonitriles 8 and pyrimidoind

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