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1722-89-0

Acetamide, N-(2,2-diphenylethenyl)-, also known as 2,2-diphenylvinyl acetamide, is an organic compound with the chemical formula C18H15NO. It is a derivative of acetamide, featuring a 2,2-diphenylethenyl group attached to the nitrogen atom. Acetamide, N-(2,2-diphenylethenyl)- is characterized by its aromatic structure, with two phenyl rings (C6H5) connected to a vinyl group (C=C), which is in turn bonded to the acetamide moiety. It is a white crystalline solid and is used in various chemical and pharmaceutical applications, such as the synthesis of other organic compounds and as an intermediate in the production of certain pharmaceuticals. Due to its specific structure, it may exhibit unique chemical properties and reactivity compared to other acetamide derivatives.

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  • 1722-89-0 Structure

  • Basic information

    1. Product Name: Acetamide, N-(2,2-diphenylethenyl)-
    2. Synonyms:
    3. CAS NO:1722-89-0
    4. Molecular Formula: C16H15NO
    5. Molecular Weight: 237.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1722-89-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Acetamide, N-(2,2-diphenylethenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, N-(2,2-diphenylethenyl)-(1722-89-0)
    11. EPA Substance Registry System: Acetamide, N-(2,2-diphenylethenyl)-(1722-89-0)

  • 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: 1722-89-0(Hazardous Substances Data)

1722-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1722-89-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1722-89:
(6*1)+(5*7)+(4*2)+(3*2)+(2*8)+(1*9)=80
80 % 10 = 0
So 1722-89-0 is a valid CAS Registry Number.

1722-89-0SDS

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 N-(2,2-diphenylethenyl)acetamide

1.2 Other means of identification

Product number -
Other names 2-<Methyl-acetyl-amino>-1,1-diphenyl-aethylen

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:1722-89-0 SDS

1722-89-0Relevant articles and documents

Direct titanium-mediated conversion of ketones into enamides with ammonia and acetic anhydride

Reeves, Jonathan T.,Tan, Zhulin,Han, Zhengxu S.,Li, Guisheng,Zhang, Yongda,Xu, Yibo,Reeves, Diana C.,Gonnella, Nina C.,Ma, Shengli,Lee, Heewon,Lu, Bruce Z.,Senanayake, Chris H.

supporting information; experimental part, p. 1400 - 1404 (2012/03/26)

A one-step conversion of ketones into N-acetyl enamides was developed. The process employs safe and inexpensive reagents, proceeds under mild conditions, and tolerates diverse functional groups. The addition of edte (N,N,N ,N -tetrakis(2-hydroxyethyl)ethy

Reduction of 2,2-Diaryl-1-nitroethylenes : New Synthesis of 2,2-Diarylacetaldehydes and 1,1,4,4-Tetraarylbuta-1,3-dienes

Tadros, Wadie,Awad, Sami B.,Sakla, Alfy B.,Abdul-Malik, Nadia F.,Armanious, Emili R.

, p. 199 - 202 (2007/10/02)

2,2-Diarylacetaldehydes (VII) have been obtained by selective and controlled reduction of 2,2-diaryl-1-nitroethylenes (IV) in acid medium, and also by acid hydrolysis of 2,2-diarylvinyl-N-acetamides (VI).Nitroalkenes (IV) have been prepared by the reaction of 2,2-diarylethylenes (I) with nitrous acid whereas N-acetamide derivatives (VI) have been obtained by reductive acetylation of the nitro compounds (IV).A number of 1,1,4,4-tetraarylbuta-1,3-dienes (XI) have been obtained by the condensation of 2,2-diarylacetaldehydes (VII) with appropriate 2,2-diarylethylenes (I).Structures of the products have been assigned on the basis of analytical data and chemical and spectral evidences.

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