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1-Benzyl-3-pyrrolidinone / 25g

Purity: 98 %
Synonym: 1-benzylpyrrolidin-3-one; N-Benzyl-3-pyrrolidone; 1-(Phenylmethyl)-3-pyrrolidinone
Molecular Formula: C11H13NO
Molecular Weight: 175.23
SKU: MND-121259
CAS Number: 775-16-6
MDL number: MFCD00005342
EC Number: 212-274-0
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 25g  
400.40 EUR



Safety Information


Hazard Statements

H315
H319
H335

Precautionary Statements

P280
P261
P271
P312
P264b
P302 + P352
P304 + P340
P305 + P351 + P338
P362 + P364
P403 + P233
P501c

Pictograms



Properties

Density1.091
Boiling Point77-78°/0.01mm

 Product Description

1-Benzyl-3-pyrrolidinone is a chemical compound utilized as a versatile intermediate in organic synthesis, known for its reactivity and structural significance in the production of pharmaceuticals, agrochemicals, and specialty chemicals.

 

Application:

It is commonly employed as a building block in the synthesis of pharmaceuticals, particularly in the formation of heterocyclic compounds, and in the manufacture of specialty chemicals for various industrial applications.

 

 

Articles:

- A Facile One-Pot Synthesis of New Poly Functionalized Pyrrolotriazoles via a Regioselective Multicomponent Cyclisation and Suzuki–Miyaura Coupling Reactions

Publication Date: 27 July 2022

Simon Garnier, Kévin Brugemann, Agnieszka Zak, Johnny Vercouillie, Marie Potier-Cartereau, Mathieu Marchivie, Sylvain Routier and Frédéric Buron

https://doi.org/10.3390/catal12080828

 

- Gene mining-based identification of aldo–keto reductases for highly stereoselective reduction of bulky ketones

Publication Date: 16 July 2018

Chen Liang, Yao Nie, Xiaoqing Mu & Yan Xu

https://doi.org/10.1186/s40643-018-0220-x

 

- A thermodynamic study of ketoreductase-catalyzed reactions 5. Reduction of substituted ketones in n-hexane

Publication Date: Available online 7 November 2007

Yadu B. Tewari, David J. Vanderah, Michele M. Schantz, Robert N. Goldberg, J. David Rozzell, Joel F. Liebman, Raymond Wai-Man Hui, Yitzy Nissenbaum, Ahmad Reza Parniani

https://doi.org/10.1016/j.jct.2007.10.011