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N-(9-ethyl-9H-carbazol-3-yl)-3-oxobutanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

331713-74-7

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331713-74-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 331713-74-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,7,1 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 331713-74:
(8*3)+(7*3)+(6*1)+(5*7)+(4*1)+(3*3)+(2*7)+(1*4)=117
117 % 10 = 7
So 331713-74-7 is a valid CAS Registry Number.

331713-74-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(9-ethylcarbazol-3-yl)-3-oxobutanamide

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:331713-74-7 SDS

331713-74-7Downstream Products

331713-74-7Relevant academic research and scientific papers

Reactions of 9-alkyl-3-aminocarbazoles with Ethyl-3-oxobutanoate and Identification of the Products Obtained

Sapijanskaite, Birute,Mickevicius, Vytautas,Mikulskiene, Gema

, p. 72 - 80 (2006)

The reactions in benzene of 9-alkyl-3-aminocarbazoles with ethyl-3-oxobutanoate yielded ethyl-3-[(9-alkyl-9H-carbazol-3-yl)amino]but-2- enoate condensation products or N-(9-ethyl-9H-carbazol-3-yl)-3-oxobutanamide acylation products. The condensation products were cyclized to the corresponding 4,7-dihydro-pyrido[2,3-c]-carbazol-1-ones upon heating in mineral oil at 240-250 °C. The structures of the synthesized compounds were investigated by IR, mass spectrometry, 1H- and 13C-NMR spectroscopy and MM2 molecular mechanics and AM1 semi-empirical quantum mechanical methods.

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