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3-Methyl-6-benzofuranol, also known as 6-benzofuranol, 3-methyl-, is an organic compound with the chemical formula C10H10O2. It is a derivative of benzofuran, a heterocyclic aromatic compound consisting of a benzene ring fused to a furan ring. The 3-methyl group in 6-Benzofuranol, 3-methyl- is attached to the benzofuran structure, specifically at the third carbon position. 3-Methyl-6-benzofuranol is a colorless to pale yellow solid and is used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the synthesis of natural products and as a building block in the development of new materials.

3652-66-2

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3652-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3652-66-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,5 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3652-66:
(6*3)+(5*6)+(4*5)+(3*2)+(2*6)+(1*6)=92
92 % 10 = 2
So 3652-66-2 is a valid CAS Registry Number.

3652-66-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1-benzofuran-6-ol

1.2 Other means of identification

Product number -
Other names 6-Benzofuranol,3-methyl

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:3652-66-2 SDS

3652-66-2Relevant academic research and scientific papers

Anion-accelerated palladium-mediated intramolecular cyclizations: Synthesis of benzofurans, indoles, and a benzopyran

Hennings, D. David,Iwasa, Seiji,Rawal, Viresh H.

, p. 6379 - 6382 (2007/10/03)

Substituted benzo-fused heterocycles such as indoles, benzofurans, and a benzopyran were obtained using an intramolecular cross-coupling of vinyl halides with phenols. This transformation represents a new route to these heterocycles and is accomplished using a palladacyclic catalyst under anionic conditions.

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