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1670-89-9

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1670-89-9 Usage

General Description

1H-Indole-7-carboyxamide, also known as 9CI, is a type of chemical compound which is a derivative of indole. Its chemical formula is C9H8N2O and molecular weight is 160.17g/mol. Indole derivatives like 9CI are often commonly used in a wide variety of chemical and pharmaceutical research due to their bioactive properties. They have potential applications in drug discovery, medicinal chemistry, and organic synthesis. Often used as synthetic intermediates, they can be utilized to produce various kinds of biologically active compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1670-89-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,7 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1670-89:
(6*1)+(5*6)+(4*7)+(3*0)+(2*8)+(1*9)=89
89 % 10 = 9
So 1670-89-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O/c10-9(12)7-3-1-2-6-4-5-11-8(6)7/h1-5,11H,(H2,10,12)

1670-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-indole-7-carboxamide

1.2 Other means of identification

Product number -
Other names 1H-Indole-7-carboxylic acid amide

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:1670-89-9 SDS

1670-89-9Downstream Products

1670-89-9Relevant articles and documents

Some Observations on the Formation of 1-Hydroxyindoles in the Leimgruber-Batcho Indole Synthesis

Clark, Robin D.,Repke, David B.

, p. 121 - 125 (2007/10/02)

The factors influencing the formation of 1-hydroxyindoles in the catalytic hydrogenation of β-dimethylamino-2-nitrostyrenes (Leimgruber-Batcho indole synthesis) have been investigated.Significant amounts of 1-hydroxyindoles were obtained only when the β-dimethylamino-2-nitrostyrene was substituted with an electron-withdrawing group at the 5 or 6 position.The proportion of 1-hydroxyindole formed relative to the normal indole product was found to increase as both the amount of catalyst and hydrogen pressure were decreased.

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