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7-Bromo-2,3-dimethyl-1-benzofuran is an organic chemical compound characterized by a benzofuran ring structure, which is a fusion of a benzene ring and a furan ring. This particular compound is distinguished by the presence of a bromine atom at the 7th position, and two methyl groups at the 2nd and 3rd positions. It is a colorless to pale yellow solid with a molecular formula of C10H9BrO. 7-BROMO-2,3-DIMETHYL-1-BENZOFURAN is often used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is important to handle this chemical with care, as it may have potential health and environmental impacts, and is typically used in a controlled laboratory setting.

5791-90-2

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5791-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5791-90-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,9 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5791-90:
(6*5)+(5*7)+(4*9)+(3*1)+(2*9)+(1*0)=122
122 % 10 = 2
So 5791-90-2 is a valid CAS Registry Number.

5791-90-2SDS

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 7-bromo-2,3-dimethyl-1-benzofuran

1.2 Other means of identification

Product number -
Other names 7-bromo-2,3-dimethyl-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:5791-90-2 SDS

5791-90-2Downstream Products

5791-90-2Relevant academic research and scientific papers

A Gold(I) Complex with a 1,1′-Binaphthyl-Substituted Diphosphene: Synthesis, Structure, and Catalytic Application to Intramolecular Hydroarylation Reactions

Kamikawa, Ken,Tsurusaki, Akihiro,Ura, Rikako

, (2019)

A gold(I) complex with a 1,1′-binaphthyl-substituted diphosphene was synthesized and fully characterized. A phosphorus atom with a less-hindered binaphthyl group coordinates to a gold(I) moiety in an η1 fashion. Both experiment and theoretical calculations supported the facile rotation around the C(Naph)-P bond in neutral and cationic diphosphene-gold(I) complexes. The newly obtained complex 2 was applied to the intramolecular hydroarylation of aryl propynyl ethers 5, and 2H-chromenes 6 were formed in 83-94% yield. Furthermore, the chiral diphosphene-gold(I) complex (S)-2 was used in the atropselective reaction to furnish 6b,c with up to 9% ee, which is the first example of the use of a diphosphene as a ligand for the transition-metal-catalyzed organic transformation.

2-aminoethyl-benzofuran derivatives, preparation thereof and therapeutical use thereof

-

, (2011/05/18)

PCT No. PCT/FR97/00383 Sec. 371 Date Aug. 31, 1998 Sec. 102(e) Date Aug. 31, 1998 PCT Filed Mar. 5, 1997 PCT Pub. No. WO97/32870 PCT Pub. Date Sep. 12, 1997Compounds of formula (I), wherein A is a hydrogen atom or a hydroxyl group; B is a hydrogen atom or

Benzylamine derivatives, their preparation and their application in therapeutics

-

, (2008/06/13)

Compounds of general formula (I) STR1 in which: A represents either a hydrogen atom, a hydroxyl, a C1-6 hydroxyalkyl group, a thiol, a C1-6 alkylsulphanyl group, an amino group, a C1-6 alkylamino group, a di(C1-6/sub

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