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13391-28-1

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13391-28-1 Usage

Synthesis Reference(s)

Synthetic Communications, 19, p. 257, 1989 DOI: 10.1080/00397918908050977

Check Digit Verification of cas no

The CAS Registry Mumber 13391-28-1 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, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13391-28:
(7*1)+(6*3)+(5*3)+(4*9)+(3*1)+(2*2)+(1*8)=91
91 % 10 = 1
So 13391-28-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O2/c1-10-8-2-3-9-7(6-8)4-5-11-9/h2-6H,1H3

13391-28-1SDS

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-Methoxybenzofuran

1.2 Other means of identification

Product number -
Other names 5-methoxy-1-benzofuran

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:13391-28-1 SDS

13391-28-1Relevant articles and documents

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Trofimov et al.

, (1973)

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Copper-Catalyzed Methoxylation of Aryl Bromides with 9-BBN-OMe

Li, Chen,Song, Zhi-Qiang,Wang, Dong-Hui,Wang, Jing-Ru

supporting information, p. 8450 - 8454 (2021/11/17)

A Cu-catalyzed cross-coupling reaction between aryl bromides and 9-BBN-OMe to provide aryl methyl ethers under mild conditions is reported. The oxalamide ligand BHMPO plays a key role in the transformation. Various functional groups on bromobenzenes are well tolerated, providing the desired anisole products in moderate to high yields.

Method suitable for large-scale production of B-RAF kinase dimer inhibitor

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Paragraph 0065-0066, (2020/08/18)

The invention relates to a method for large-scale production of a B-RAF kinase dimer inhibitor 1-((1S, 1aS, 6bS)-5-((7-oxo-5, 6, 7, 8-tetrahydro-1, 8-diazanaphthalene-4-yl) oxy)-1a, 6b-dihydro-1H-cyclopropyl [b] benzofuran-1-yl)-3-(2, 4, 5- trifluorophenyl) urea (hereinafter sometimes referred to as a compound 1). The method enables impurities or by-products to be controlled to 0.05% or less without the use of expensive column chromatography operations. Thus, the method greatly reduces cost and is suitable for large-scale production.

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