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6209-23-0

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6209-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6209-23-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,0 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6209-23:
(6*6)+(5*2)+(4*0)+(3*9)+(2*2)+(1*3)=80
80 % 10 = 0
So 6209-23-0 is a valid CAS Registry Number.

6209-23-0SDS

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 ethyl 2-carbazol-9-ylacetate

1.2 Other means of identification

Product number -
Other names ethyl 2-(9H-carbazol-9-yl)acetate

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:6209-23-0 SDS

6209-23-0Relevant articles and documents

Synthesis, characterization and biological evaluation of some newer carbazole derivatives

Sharma, Divyanshu,Kumar, Nitin,Pathak, Devender

, p. 125 - 132 (2014)

A series of novel 5-[(9H-carbazol-9-yl)methyl]-N-[(substituted phenyl)( piperazin-1-yl)methyl]-1,3,4-oxadiazol-2-amines (4a-o) derivatives was synthesized by starting with carbazole, which on reaction with ethyl chloroacetate yielded ethyl 2-(9H-carbazole

OFF-ON-OFF Dual Emission at Visible and UV Wavelengths from Carbazole Functionalized β-Diketonate Europium(III) Complex

Imai, Yuki,Kawai, Tsuyoshi,Yuasa, Junpei

, p. 4131 - 4138 (2016)

This work demonstrates dual emission "OFF-ON-OFF" switching at visible and UV wavelengths of a carbazole functionalized β-diketone (LH) by a simple change of a europium(III) ion (Eu3+) concentration in the submicromolar concentration range. In

Carbazole-isatin type compound and preparation method and application thereof

-

Paragraph 0010, (2016/10/08)

The invention discloses a carbazole-isatin type compound and a preparation method and application thereof.The compound is of a structure as shown in a formula (I), and the preparation method comprises the steps of using carbazole and ethyl bromoacetate as raw materials to obtain 2-(9H-carbazole-9-yl) ethyl acetate, then performing hydrazinolysis reaction to obtain 2-(9H-carbazole-9-yl) acethydrazide, and finally performing reaction with various types of substitutive isatin to obtain a target compound.The compound can serve as a raw material for anti-tumor drugs, the raw materials for the preparation method are simple and easy to obtain, and operation is convenient.

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