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2-Pyrrolidinone,3-(hydroxymethyl)-1-methyl-(9CI) is a versatile chemical compound characterized by a pyrrolidone ring with a substituted hydroxymethyl and methyl group. Its unique structural features and functional groups contribute to its reactivity and stability, making it an essential building block in the synthesis of pharmaceuticals, agrochemicals, and polymers. Additionally, it serves as a solvent and reagent in organic synthesis, further expanding its applications in various industries.

577780-05-3

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577780-05-3 Usage

Uses

Used in Pharmaceutical Industry:
2-Pyrrolidinone,3-(hydroxymethyl)-1-methyl-(9CI) is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and functional groups enable the development of novel drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Pyrrolidinone,3-(hydroxymethyl)-1-methyl-(9CI) is utilized as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its versatile reactivity allows for the creation of effective and environmentally friendly products.
Used in Polymer Industry:
2-Pyrrolidinone,3-(hydroxymethyl)-1-methyl-(9CI) is employed as a monomer or a comonomer in the production of polymers with specific properties. Its incorporation into polymer chains can enhance the material's performance, making it suitable for various applications, such as coatings, adhesives, and plastics.
Used as a Solvent in Organic Synthesis:
Due to its ability to dissolve a wide range of compounds, 2-Pyrrolidinone,3-(hydroxymethyl)-1-methyl-(9CI) is used as a solvent in various organic synthesis processes. Its solubility properties facilitate the reaction of different substrates, leading to improved yields and reaction efficiency.
Used as a Reagent in Organic Synthesis:
2-Pyrrolidinone,3-(hydroxymethyl)-1-methyl-(9CI) also serves as a reagent in organic synthesis, enabling the formation of new chemical bonds and the modification of existing ones. Its unique functional groups allow for a wide range of reactions, making it a valuable tool for researchers and industrial chemists in the development of novel materials and pharmaceutical products.

Check Digit Verification of cas no

The CAS Registry Mumber 577780-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,7,7,8 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 577780-05:
(8*5)+(7*7)+(6*7)+(5*7)+(4*8)+(3*0)+(2*0)+(1*5)=203
203 % 10 = 3
So 577780-05-3 is a valid CAS Registry Number.

577780-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Hydroxymethyl)-1-methylpyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names 3-(hydroxymethyl)-1-methylpyrrolidin-2-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:577780-05-3 SDS

577780-05-3Downstream Products

577780-05-3Relevant academic research and scientific papers

Novel spiroheterocycles by aziridination of α-methylene-γ- and -δ-lactams

Loreto, M. Antonietta,Migliorini, Antonella,Tardella, P. Antonio,Gambacorta, Augusto

, p. 2365 - 2371 (2008/02/08)

New potentially bioactive α-spiroaziridino-γ- and -δ-lactams have been prepared by treatment of α-methylene-γ- and -δ-lactams with ethyl N-([(4-nitrophenyl)sulfonyl]oxy)-carbamate (NsONHCO2Et) in the presence of CaO. These compounds, through reductive aziridine ring opening, can be intermediates for the synthesis of α- and β-aminolactams, which are useful as conformational constraints in peptides. The above procedure has been successfully extended to one α-methyleneoxindole to obtain a new spirooxindole derivative, a potential precursor of natural alkaloids. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

THIENOPYRIMIDINES, PROCESS FOR PREPARING THE SAME AND USE THEREOF

-

Page 20, (2008/06/13)

The present invention provides a thienopyrimidine compound, represented by the formula???[wherein, R1 is C1-4 alkyl, R2 is (1) phenyl optionally having a substituent such as amino, mono C1-4 alkylamino and di C1-4 alkylamino, or (2) a heterocyclic group optionally having a substituent such as amino, mono C1-4 alkylamino and di C1-4 alkylamino and the like, R3 is a hydrogen atom or C1-4 alkyl, R4 is C1-4 alkyl optionally having a substituent such as C1-4 alkoxy-carbonyl, carboxyl, mono C1-4 alkylamino and N-C1-4 alkyl-N-C7-10 aralkylamino and the like] or a salt thereof, which has antagonistic action for gonadotropin-releasing hormone.

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