1-phenylpent-1-en-3-one

Base Information

  • Chemical Name: 1-phenylpent-1-en-3-one
  • CAS No.: 3152-68-9

Cost-effective and customizable 1-phenylpent-1-en-3-one 3152-68-9 for sale

  • Molecular Formula: C11H12 O
  • Molecular Weight: 160.216
  • Vapor Pressure: 0.00471mmHg at 25°C 
  • Melting Point: 38.5°C 
  • Refractive Index: 1.5684 
  • Boiling Point: 276.8°Cat760mmHg 
  • Flash Point: 99.6°C 
  • PSA： 17.07000 
  • Density: 0.997g/cm3 
  • LogP: 2.67890 

1-phenylpent-1-en-3-one(Cas 3152-68-9) Usage

Type of compound

Ketone
It is a ketone because it has a carbonyl group (C=O) bonded to two carbon atoms.

Presence of phenyl group

Yes
A phenyl group (a ring of 6 carbon atoms with alternating single and double bonds) is attached to the pentene chain.

Chain structure

Pentene chain
The compound has a 5-carbon chain with a double bond between two of the carbon atoms.

Physical state

Colorless liquid
1-Phenylpent-1-en-3-one is a liquid that is colorless in appearance.

Odor

Sweet floral
The compound has a pleasant, sweet floral scent.

Use in organic synthesis

Yes
1-Phenylpent-1-en-3-one is used as a reagent in chemical reactions due to its ability to undergo aldol condensation and other organic reactions.

Application in fragrance industry

Yes
The sweet floral odor of 1-phenylpent-1-en-3-one makes it suitable for use in the fragrance industry.

Use in pharmaceutical production

Yes
The compound is used in the production of pharmaceuticals, contributing to the development of various medications.

Use as a flavoring agent

Yes
1-Phenylpent-1-en-3-one is used as a flavoring agent in the food industry, enhancing the taste and aroma of various food products.

Importance in organic chemistry

High
Due to its diverse applications in various industries, 1-phenylpent-1-en-3-one is a valuable chemical in organic chemistry.

General Description

1-Phenylpent-1-en-3-one is a chemical compound with the molecular formula C11H12O. It is a ketone with a phenyl group attached to a pentene chain. 1-phenylpent-1-en-3-one is used in organic synthesis and as a reagent in chemical reactions due to its ability to undergo aldol condensation and other organic reactions. It is a colorless liquid with a sweet floral odor and is used in the fragrance industry as well. Additionally, 1-phenylpent-1-en-3-one is also used in the production of pharmaceuticals and as a flavoring agent in the food industry. Due to its diverse applications, this compound plays an important role in various industries and is a valuable chemical in organic chemistry.

InChI:InChI=1/C11H12O/c1-2-11(12)9-8-10-6-4-3-5-7-10/h3-9H,2H2,1H3/b9-8+

3152-68-9 Relevant articles

-

Gettler,Hammett

, p. 1824,1825 (1943)

-

Gold(I)-catalyzed ring expansion of cyclopropanols and cyclobutanols

Markham, Jordan P.,Staben, Steven T.,Toste, F. Dean

, p. 9708 - 9709 (2005)

The rearrangement of 1-alkynyl cyclobuta...

An Expedient Synthesis of α,β-Unsaturated Ketones Using Nitroalkenes and Sulfones

Awen, Bahlul Z.,Miyashita, Masaaki,Shiratani, Tomonori,Yoshikoshi, Akira,Irie, Hiroshi

, p. 767 - 768 (1992)

A facile synthesis of various substitute...

Contemporaneous Dual Catalysis: Aldol Products from Non-Carbonyl Substrates

Trost, Barry M.,Tracy, Jacob S.

, p. 15108 - 15112 (2015)

The aldol reaction represents an importa...

Chemoselective reduction of ?,￠-unsaturated carbonyl and carboxylic compounds by hydrogen iodide

Matsumoto, Shoji,Marumoto, Hayato,Akazome, Motohiro,Otani, Yasuhiko,Kaiho, Tatsuo

, p. 590 - 599 (2021/03/29)

The selective reduction of ?,￠-unsaturat...

Mizoroki-Heck Reaction of Unstrained Aryl Ketones via Ligand-Promoted C-C Bond Olefination

Wang, Mei-Ling,Xu, Hui,Li, Han-Yuan,Ma, Biao,Wang, Zhen-Yu,Wang, Xing,Dai, Hui-Xiong

, p. 2147 - 2152 (2021/04/05)

Mizoroki-Heck reaction of unstrained ary...

A Heck reaction/photochemical alkene isomerization sequence to prepare functionalized quinolines

Donohoe, Timothy J.,Hoff, Oskar,Hoffman, Jack B.,Kelly, Alex,Walker, Johannes C. L.,Werrel, Simon

, (2020/08/06)

A route to prepare functionalized quinol...

Pd-catalyzed oxidative Heck-type arylation of vinyl ketones, alkenes, and acrylates with Sb-aryl-tetrahydrodibenz[c,f][1,5]azastibocines

Murata, Yuki,Kakusawa, Naoki,Arakawa, Yukako,Hayashi, Yukako,Morinaga, Shun,Ueda, Masaaki,Hyodo, Tadashi,Matsumura, Mio,Yamaguchi, Kentaro,Kurita, Jyoji,Yasuike, Shuji

, (2020/10/18)

The Pd-catalyzed cross-coupling reaction...

3152-68-9 Process route

1-(trimethylsilyl)-2-phenylethene
19372-00-0

1-(trimethylsilyl)-2-phenylethene

propionic acid anhydride
123-62-6

propionic acid anhydride

styrene
100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6

styrene

(1E)-1-phenylpent-1-en-3-one
3152-68-9

(1E)-1-phenylpent-1-en-3-one

Conditions
Conditions Yield
With bis(1,5-cyclooctadiene)diiridium(I) dichloride; In toluene; at 120 ℃; for 24h; Inert atmosphere;
58%
1-hydroxy-1-phenylpentan-3-one
37038-75-8

1-hydroxy-1-phenylpentan-3-one

1-phenyl-pent-1-en-3-one
3152-68-9

1-phenyl-pent-1-en-3-one

benzaldehyde
100-52-7

benzaldehyde

Conditions
Conditions Yield
at 25 ℃; Rate constant;

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