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ethyl 5-chloro-3-phenyl-1-benzofuran-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27006-00-4

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27006-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27006-00-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,0 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27006-00:
(7*2)+(6*7)+(5*0)+(4*0)+(3*6)+(2*0)+(1*0)=74
74 % 10 = 4
So 27006-00-4 is a valid CAS Registry Number.

27006-00-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-chloro-3-phenyl-1-benzofuran-2-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 5-chloro-3-phenylbenzofuran-2-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:27006-00-4 SDS

27006-00-4Relevant academic research and scientific papers

Convenient synthesis of some 3-phenyl-1-benzofuran-2-carboxylic acid derivatives as new potential inhibitors of ClC-Kb channels

Piemontese, Luca,Carbonara, Giuseppe,Fracchiolla, Giuseppe,Laghezza, Antonio,Tortorella, Paolo,Loiodice, Fulvio

experimental part, p. 2865 - 2872 (2011/04/24)

Improved experimental conditions were carried out for the preparation in high yields of some 3-phenyl-1-benzofuran-2-carboxylic acids, potent inhibitors of ClC-K chloride channels. A one-pot condensation-cyclization was set up starting from different 2-hy

One-pot synthesis of N-methylindoles from N-methylanilines and of benzofurans from phenols using transition-metal carbene X-H insertion reactions

Honey, Mark A.,Blake, Alexander J.,Campbell, Ian B.,Judkins, Brian D.,Moody, Christopher J.

experimental part, p. 8995 - 9001 (2010/03/01)

Transition-metal carbene X-H insertion reactions (X=N or O) have been employed in the simple conversion of anilines and phenols into indoles and benzofurans, respectively. Thus copper(II) catalyzed N-H insertion reactions of α-diazo-β-ketoesters with N-me

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