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5-methoxy-2,3-dihydrobenzofuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13391-30-5

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13391-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13391-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,9 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13391-30:
(7*1)+(6*3)+(5*3)+(4*9)+(3*1)+(2*3)+(1*0)=85
85 % 10 = 5
So 13391-30-5 is a valid CAS Registry Number.

13391-30-5SDS

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 5-Methoxy-2,3-dihydro-1-benzofur

1.2 Other means of identification

Product number -
Other names 2H,8H-Benzo(1,2-b,3,4-b')dipyran-8-one,5-methoxy-2,2-dimethyl-6-(2-methylcrotonoyl)-10-phenyl-,(E)

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:13391-30-5 SDS

13391-30-5Relevant academic research and scientific papers

The Synthesis of 5-Substituted 2,3-Dihydrobenzofurans

Alabaster, Ramon J.,Cottrell, Ian F.,Marley, Hugh,Wright, Stanley H. B.

, p. 950 - 952 (2007/10/02)

The preparation of 2,3-dihydrobenzofurans 6 from 2-(2-bromophenoxy)ethyl chlorides 3 by reaction with magnesium in a development of the Parham cyclialkylation reaction is described.A high yielding procedure using phase-transfer catalysis has also been developed for the preparation of the intermediate chloroethyl ethers 3 from bromophenols 2.The 5-hydroxy derivative 15 may be obtained from 2,3-dihydrobenzofuran (6a) by reaction with electrophilic reagents followed by oxidation.

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