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2-acetyl-2-allyl-γ-butyrolactone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114709-93-2

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114709-93-2 Usage

General Description

2-acetyl-2-allyl-γ-butyrolactone, also known as ACETYLLACTONE, is a chemical compound with a molecular formula of C9H12O3. It is an organic compound commonly used in the production of flavorings and fragrances due to its pleasant, sweet, and fruity odor. It is also used as a flavoring agent in the food and beverage industry, especially in the production of baked goods, candies, and ice cream. Additionally, it has been investigated for its potential pharmaceutical properties, such as its ability to act as an antitumor agent. However, further research is needed to fully understand its potential medical applications. Overall, 2-acetyl-2-allyl-γ-butyrolactone is a versatile chemical with a wide range of applications in the food, fragrance, and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 114709-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,7,0 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 114709-93:
(8*1)+(7*1)+(6*4)+(5*7)+(4*0)+(3*9)+(2*9)+(1*3)=122
122 % 10 = 2
So 114709-93-2 is a valid CAS Registry Number.

114709-93-2Downstream Products

114709-93-2Relevant academic research and scientific papers

Remarkable rate enhancement of palladium-catalyzed allylic alkylation in water using a colloidal dispersion system

Kobayashi,Lam,Manabe

, p. 6115 - 6119 (2000)

The rate of palladium-catalyzed allylic alkylation was dramatically enhanced in a colloidal dispersion system created by a neutral surfactant, Triton X-100, in water. (C) 2000 Elsevier Science Ltd.

Studies on the diastereo-selective reduction of 2-acetyl-2-alkyl-γ-butyrolactones with boron hydrides

Teixeira, Lis H.P.,De Souza, Maria Cecilia B.V.,Ramos, Maria Da Conceicao K.V.,De Aquino Neto, Francisco R.,Barreiro, Eliezer J.,Fraga, Carlos A.M.

, p. 505 - 526 (2002)

Reduction of 2-acetyl-2-alkyl-γ-butyrolactone derivatives with boron hydrides in the presence and absence of several chelating agents were studied. This process is influenced more by steric than chelation factors, yielding the isomeric alcohols syn (13-23

Direct Allylation of Active Methylene Compounds with Allylic Alcohols by Use of Palladium/Phosphine-Borane Catalyst System

Shimizu, Aika,Hirata, Goki,Onodera, Gen,Kimura, Masanari

supporting information, p. 1954 - 1960 (2018/04/11)

The C?C bond formation between active methylene compounds and allylic alcohols has been newly developed by using a palladium complex as a catalyst together with a phosphine-borane ligand. The best phosphine-borane ligand for this direct allylation has bee

N-Heterocyclic olefins as efficient phase-transfer catalysts for base-promoted alkylation reactions

Blümel, Marcus,Crocker, Reece D.,Harper, Jason B.,Enders, Dieter,Nguyen, Thanh V.

supporting information, p. 7958 - 7961 (2016/07/06)

N-Heterocyclic olefins (NHOs) have very recently emerged as efficient promoters for several chemical reactions due to their strong Br?nsted/Lewis basicities. Here we report the novel application of NHOs as efficient phase-transfer organocatalysts for synt

Triethylborane as an efficient promoter for palladium-catalyzed allylation of active methylene compounds with allyl alcohols

Kimura, Masanari,Mukai, Ryutaro,Tanigawa, Naoko,Tanaka, Shuji,Tamaru, Yoshinao

, p. 7767 - 7777 (2007/10/03)

Without prior activation of allyl alcohols, allylation of a variety of active methylene compounds with allyl alcohols proceeds smoothly at rt-50°C in the presence of catalytic amounts of Pd(OAc)2 (1-10mol%), Et 3B (30-240mol%), a phosphine ligand (1-20mol%), and a base (0 to 50-60mol%).

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