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9H-Carbazole-3-carboxylic acid, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51035-14-4

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51035-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51035-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,3 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51035-14:
(7*5)+(6*1)+(5*0)+(4*3)+(3*5)+(2*1)+(1*4)=74
74 % 10 = 4
So 51035-14-4 is a valid CAS Registry Number.

51035-14-4SDS

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 9H-carbazole-3-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names ethyl carbazole-3-carboxylate

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:51035-14-4 SDS

51035-14-4Relevant academic research and scientific papers

A novel synthesis of N-protected carbazoles involving electrocyclization of in situ generated enamines

Mohanakrishnan, Arasambattu K.,Balamurugan, Ramalingam

, p. 4045 - 4048 (2005)

A new route for the synthesis of carbazoles has been realized through the intermediacy of 2,3-divinylindoles involving an electrocyclization followed by aromatization.

Synthesis of substituted carbazoles via electrocyclization of in situ generated enamines from 1-phenylsulfonyl-2/(3)-methyl-3/(2)-vinylindoles and DMF·DMA/DMA·DMA

Sureshbabu, Radhakrishnan,Balamurugan, Ramalingam,Mohanakrishnan, Arasambattu K.

scheme or table, p. 3582 - 3591 (2009/09/08)

Interaction of 2/(3)-methyl-3/(2)-vinylindoles and DMF·DMA/DMA·DMA at 110 °C led to the in situ generation of enamines, which on concurrent electrocyclization followed by subsequent aromatization afforded substituted carbazoles.

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