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1,2,3,4-tetrahydro-9H-carbazole-9-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67242-61-9

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67242-61-9 Usage

Core structure

Tetrahydro-9H-carbazole

Substituent

Carboxamide group attached to the ninth carbon atom

Derivative

Carbazole

Biological and pharmacological activities

Potential use as a building block in the synthesis of medicinal compounds, ligand in coordination chemistry, anti-cancer agent, and neuroprotective properties.

Electronic and photophysical properties

Potential use in organic optoelectronic devices.

Check Digit Verification of cas no

The CAS Registry Mumber 67242-61-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,4 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67242-61:
(7*6)+(6*7)+(5*2)+(4*4)+(3*2)+(2*6)+(1*1)=129
129 % 10 = 9
So 67242-61-9 is a valid CAS Registry Number.

67242-61-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4-tetrahydrocarbazole-9-carboxamide

1.2 Other means of identification

Product number -
Other names 1,2,3,4-Tetrahydro-9H-carbazole-9-carboxamide

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:67242-61-9 SDS

67242-61-9Downstream Products

67242-61-9Relevant academic research and scientific papers

An efficient synthesis of 1,1-disubstituted hydrazines

Murakami,Yokoyama,Sasakura,Tamagawa

, p. 423 - 428 (2007/10/02)

1,1-disubstituted hydrazines were prepared from the corresponding 1,1-disubstituted ureas by means of the Hofmann rearrangement reaction. The yields were fairly good, except from the ureas susceptible to oxidation, and thus the present method represents an additional and efficient procedure for the synthesis of 1,1-disubstituted hydrazines.

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