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143797-94-8

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143797-94-8 Usage

Type of compound

Chemical compound

Derivative of

Indole

Found in

Plants and animals

Use

Synthesis of pharmaceuticals and other organic compounds

Known for

Potential use as an intermediate in the production of dyes, pigments, and other industrial chemicals

Studied for

Potential pharmacological properties

Ability

To act as an inhibitor of certain enzymes

Applications

Wide-ranging in both the chemical and pharmaceutical industries

Check Digit Verification of cas no

The CAS Registry Mumber 143797-94-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,7,9 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 143797-94:
(8*1)+(7*4)+(6*3)+(5*7)+(4*9)+(3*7)+(2*9)+(1*4)=168
168 % 10 = 8
So 143797-94-8 is a valid CAS Registry Number.

143797-94-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3-trimethylindol-5-amine

1.2 Other means of identification

Product number -
Other names 5-amino-1,2,3-trimethylindole

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:143797-94-8 SDS

143797-94-8Relevant articles and documents

One-pot synthesis of pyrrolo[3,2-f]-and pyrrolo[2,3-h]quinoline derivatives: Observation of an unexpected mechanistic pathway

Ramesh, Subburethinam,Nagarajan, Rajagopal

supporting information; scheme or table, p. 717 - 722 (2012/07/03)

One-pot synthesis of pyrrolo[3,2-f]- and pyrrolo[2,3-h]quinolines were obtained starting from substituted 5-aminoindoles, benzaldehydes, and phenylacetylenes in the presence of La(OTf)3 as a catalyst in good yields. The indole moiety in 5-aminoindole is believed to be mainly responsible for the observation of unexpected mechanistic pathway to the formation of pyrrolo[2,3-h]quinoline. Georg Thieme Verlag Stuttgart · New York.

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