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3661-73-2

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3661-73-2 Usage

General Description

Benzamide, 4-ethenyl- (9CI) is a chemical compound with the molecular formula C9H9NO. It is a derivative of benzamide with an ethenyl group attached to the 4-position of the benzene ring. Benzamide, 4-ethenyl- (9CI) is a white to off-white solid that is insoluble in water but soluble in organic solvents. It is used as a building block in the synthesis of various pharmaceuticals and organic compounds. Benzamide, 4-ethenyl- (9CI) is also known for its potential biological activities, including antifungal and anti-inflammatory properties. It is important to handle this compound with care, as it may be harmful if ingested, inhaled, or exposed to the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 3661-73-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,6 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3661-73:
(6*3)+(5*6)+(4*6)+(3*1)+(2*7)+(1*3)=92
92 % 10 = 2
So 3661-73-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO/c1-2-7-3-5-8(6-4-7)9(10)11/h2-6H,1H2,(H2,10,11)

3661-73-2SDS

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 4-ethenylbenzamide

1.2 Other means of identification

Product number -
Other names Benzamide,4-ethenyl

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:3661-73-2 SDS

3661-73-2Relevant articles and documents

Nickel-Catalyzed Reductive Cross-Coupling of Aryl Bromides with Vinyl Acetate in Dimethyl Isosorbide as a Sustainable Solvent

Su, Mincong,Huang, Xia,Lei, Chuanhu,Jin, Jian

supporting information, p. 354 - 358 (2022/01/15)

A nickel-catalyzed reductive cross-coupling has been achieved using (hetero)aryl bromides and vinyl acetate as the coupling partners. This mild, applicable method provides a reliable access to a variety of vinyl arenes, heteroarenes, and benzoheterocycles, which should expand the chemical space of precursors to fine chemicals and polymers. Importantly, a sustainable solvent, dimethyl isosorbide, is used, making this protocol more attractive from the point of view of green chemistry.

Formation of Carbon-Carbon Bond on Solid Support: Application of the Stille Reaction

Deshpande, Milind S.

, p. 5613 - 5614 (2007/10/02)

Vinyl/Aryl stannanes couple smoothly with polymer bound aryl iodides.The cross-coupled products are obtained in excellent yield and purity after cleavage from the solid support.

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