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3-Benzofurancarboxaldehyde, 5-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

143883-36-7

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143883-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143883-36-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,8,8 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 143883-36:
(8*1)+(7*4)+(6*3)+(5*8)+(4*8)+(3*3)+(2*3)+(1*6)=147
147 % 10 = 7
So 143883-36-7 is a valid CAS Registry Number.

143883-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-1-benzofuran-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-METHYL-3-BENZOFURANCARBOXALDEHYDE

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:143883-36-7 SDS

143883-36-7Downstream Products

143883-36-7Relevant academic research and scientific papers

Rh(II)-Catalyzed Denitrogenative Transannulation of N-Sulfonyl-1,2,3-Triazolyl Cyclohexadienones for the Synthesis of Benzofurans and Cyclopropa[ cd]indole-carbaldehydes

Sontakke, Geetanjali S.,Pal, Kuntal,Volla, Chandra M. R.

, p. 12198 - 12208 (2019)

A rhodium-catalyzed intramolecular denitrogenative transannulation of N-sulfonyl-1,2,3-Triazole-Tethered cyclohexadienones has been achieved for the synthesis of benzofurans and cyclopropa[cd]indole-carbaldehydes in an operationally simple procedure. Rema

A convenient synthesis of benzofuran-3-carboxyaldehydes

Deshpande, A. R.,Paradkar, M. V.

, p. 526 - 528 (2007/10/02)

The benzofuran-3-acetic acids (3a-c) on treatment with pyridine N-oxide give benzofuran-3-carboxyaldehydes (5a-c) on reduction with NaBH4 in methanol yields naturally occurring benzofuran 6a which is converted into 6b and 6c by the literature method.

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