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37603-26-2

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37603-26-2 Usage

General Description

(5-METHOXY-1-BENZOFURAN-2-YL)METHANOL is a chemical compound with a molecular formula of C10H10O3. It is a benzofuran derivative with a methanol group attached to the benzofuran ring. (5-METHOXY-1-BENZOFURAN-2-YL)METHANOL is commonly used in organic synthesis and as a reagent in chemical reactions. It has potential applications in the pharmaceutical industry, particularly in the development of new drugs and medications. Its structure and properties make it a versatile and useful compound for various research and industrial purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 37603-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,0 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 37603-26:
(7*3)+(6*7)+(5*6)+(4*0)+(3*3)+(2*2)+(1*6)=112
112 % 10 = 2
So 37603-26-2 is a valid CAS Registry Number.

37603-26-2SDS

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-Methoxy-1-benzofuran-2-yl)methanol

1.2 Other means of identification

Product number -
Other names (5-methoxybenzofuran-2-yl)methanol

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:37603-26-2 SDS

37603-26-2Relevant articles and documents

A photochemical route to 2-substituted benzo[b]furans

Protti, Stefano,Fagnoni, Maurizio,Albini, Angelo

experimental part, p. 6473 - 6479 (2012/10/08)

2-Substituted benzo[b]furans were synthesized by a one-step metal-free photochemical reaction between 2-chlorophenol derivatives and terminal alkynes by tandem formation of an aryl-C and a C-O bond via an aryl cation intermediate. The mild conditions and the application to chlorophenols rather of the more expensive bromo or iodo analogues makes this procedure environmentally convenient.

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