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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. This white to off-white solid is insoluble in water but soluble in organic solvents. It is recognized for its potential biological activities, such as antifungal and anti-inflammatory properties, and is utilized as a building block in the synthesis of various pharmaceuticals and organic compounds.

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  • 3661-73-2 Structure
  • Basic information

    1. Product Name: Benzamide, 4-ethenyl- (9CI)
    2. Synonyms: Benzamide, 4-ethenyl- (9CI);4-ethenylbenzamide;4-vinylbenzamide
    3. CAS NO:3661-73-2
    4. Molecular Formula: C9H9NO
    5. Molecular Weight: 147.17386
    6. EINECS: N/A
    7. Product Categories: AMIDE
    8. Mol File: 3661-73-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 301.5 °C at 760 mmHg
    3. Flash Point: 136.2 °C
    4. Appearance: /
    5. Density: 1.097 g/cm3
    6. Vapor Pressure: 0.00105mmHg at 25°C
    7. Refractive Index: 1.603
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Benzamide, 4-ethenyl- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Benzamide, 4-ethenyl- (9CI)(3661-73-2)
    12. EPA Substance Registry System: Benzamide, 4-ethenyl- (9CI)(3661-73-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 3661-73-2(Hazardous Substances Data)

3661-73-2 Usage

Uses

Used in Pharmaceutical Industry:
Benzamide, 4-ethenyl(9CI) serves as a crucial building block in the synthesis of a variety of pharmaceuticals and organic compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, Benzamide, 4-ethenyl(9CI) is used as a versatile intermediate for creating a range of organic compounds. Its reactivity and functional groups make it a valuable component in the production of specialty chemicals.
Used in Antifungal Applications:
Due to its antifungal properties, Benzamide, 4-ethenyl(9CI) can be utilized in the development of antifungal agents. This can be particularly beneficial in treating various fungal infections and controlling the growth of fungi in different settings.
Used in Anti-inflammatory Applications:
Benzamide, 4-ethenyl(9CI) also exhibits anti-inflammatory properties, making it a potential candidate for the development of anti-inflammatory drugs. This can aid in the management of inflammation-related conditions and provide relief to patients suffering from such ailments.
It is important to handle Benzamide, 4-ethenyl(9CI) with care, as it may be harmful if ingested, inhaled, or exposed to the skin. Proper safety measures should be taken during its use to minimize any potential risks.

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.

A general and efficient heterogeneous gold-catalyzed hydration of nitriles in neat water under mild atmospheric conditions

Liu, Yong-Mei,He, Lin,Wang, Miao-Miao,Cao, Yong,He, He-Yong,Fan, Kang-Nian

scheme or table, p. 1392 - 1396 (2012/10/07)

Mild, efficient and general: Titania decorated with nanometer-sized gold particles acts as an efficient catalyst for the selective hydration of a wide range of chemically diverse nitriles into valuable amides in neutral water, under mild atmospheric conditions (see image). The process shows promise for a facile and direct one-pot synthesis of ?μ-caprolactam, an industrially important molecule, starting from 6-aminocapronitrile. Copyright

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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