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89017-55-0

2-Pyrrolidinone,5-(1,2-propadienyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 89017-55-0 Structure

  • Basic information

    1. Product Name: 2-Pyrrolidinone,5-(1,2-propadienyl)-(9CI)
    2. Synonyms: 2-Pyrrolidinone,5-(1,2-propadienyl)-(9CI)
    3. CAS NO:89017-55-0
    4. Molecular Formula: C7H9NO
    5. Molecular Weight: 123.15246
    6. EINECS: N/A
    7. Product Categories: PYRROLIDINE
    8. Mol File: 89017-55-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Pyrrolidinone,5-(1,2-propadienyl)-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Pyrrolidinone,5-(1,2-propadienyl)-(9CI)(89017-55-0)
    11. EPA Substance Registry System: 2-Pyrrolidinone,5-(1,2-propadienyl)-(9CI)(89017-55-0)

  • 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: 89017-55-0(Hazardous Substances Data)

89017-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89017-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,1 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89017-55:
(7*8)+(6*9)+(5*0)+(4*1)+(3*7)+(2*5)+(1*5)=150
150 % 10 = 0
So 89017-55-0 is a valid CAS Registry Number.

89017-55-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Propadienyl-2-pyrrolidinone

1.2 Other means of identification

Product number -
Other names 5-aldehydo-6-phenylpyridazin-3(2H)-one

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:89017-55-0 SDS

89017-55-0Relevant articles and documents

LEWIS ACID INDUCED REACTIONS OF PROPARGYL TRIMETHYL SILANE WITH ω-ETHOXY LACTAMS. SYNTHESIS OF γ-ALLENYL-GABA

Hiemstra, Henk,Fortgens, Hendrikus P.,Speckamp, W. Nico

, p. 3115 - 3118 (1984)

Reactions of propargyl trimethyl silane with ω-ethoxy lactams 1a-c under the influence of boron trifluoride etherate afford ω-allenyl lactams 3a-c; 5-allenyl-2-pyrrolidinone is hydrolyzed to γ-allenyl-GABA.

Expedient pyrrolizidine synthesis by propargylsilane addition to N-acyliminium ions followed by gold-catalyzed α-allenyl amide cyclization

Breman, Arjen C.,Dijkink, Jan,Van Maarseveen, Jan H.,Kinderman, Sape S.,Hiemstra, Henk

supporting information; experimental part, p. 6327 - 6330 (2009/12/24)

(Chemical Equation Presented) A reaction sequence, involving the addition of (substituted) propargylsilanes to lactam-derived N-acyliminium ions followed by gold-catalyzed cyclization of the resulting α-allenyl amide, is applied in expedient syntheses of

N-Acyliminium ion chemistry and palladium catalysis: A useful combination to obtain bicyclic heterocycles

Karstens, Willem F.J.,Klomp, Dirk,Rutjes, Floris P.J.T.,Hiemstra, Henk

, p. 5123 - 5130 (2007/10/03)

By using N-acyliminium ion chemistry, several ω-propadienyllactams and a propadienyloxazolidine were prepared from N-acyliminium ion precursors and propargylsilanes. Treatment of these allene containing lactams and oxazolidinone with allyl halides or an a

Process for the production of (S)-vinyl and allenyl gaba

-

, (2008/06/13)

The present invention is directed to a new class of pyrrolidinone derivatives that are useful as chemical intermediates in the synthesis of S-allenyl and S-vinyl GABA, both of which are antiepileptic agents.

γ-allenyl-γ-aminobutyric acids

-

, (2008/06/13)

This invention is for γ-allenyl-γ-aminobutyric acid derivatives which are γ-aminobutyric acid transaminase inhibitors.

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