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5-Octylfuran-2(5H)-one is a furan derivative with the molecular formula C12H18O2, featuring a butyl substituent at the 5th position. It is a chemical compound known for its sweet, caramel-like odor, making it a valuable component in the fragrance and flavor industry.

17756-68-2

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17756-68-2 Usage

Uses

Used in the Fragrance and Flavor Industry:
5-Octylfuran-2(5H)-one is used as a flavoring agent for its sweet, caramel-like odor, enhancing the taste and aroma of various food products.
Used in the Production of Perfumes and Cosmetics:
5-Octylfuran-2(5H)-one is utilized as a fragrance ingredient in perfumes and cosmetics, contributing to their pleasant and appealing scents.
Used in the Pharmaceutical Industry:
5-Octylfuran-2(5H)-one is being studied for its potential biological activities and medicinal applications, indicating its possible use as a pharmaceutical agent in the future.

Check Digit Verification of cas no

The CAS Registry Mumber 17756-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,5 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17756-68:
(7*1)+(6*7)+(5*7)+(4*5)+(3*6)+(2*6)+(1*8)=142
142 % 10 = 2
So 17756-68-2 is a valid CAS Registry Number.

17756-68-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Octyl-2(5H)-furanone

1.2 Other means of identification

Product number -
Other names 2-octyl-5-formylthiophene

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:17756-68-2 SDS

17756-68-2Relevant academic research and scientific papers

Structure-activity studies of cerulenin analogues as protein palmitoylation inhibitors

Lawrence, David S.,Zilfou, Jack T.,Smith, Charles D.

, p. 4932 - 4941 (1999)

Activation of ras oncogenes occurs in a high percentage of tumors, making the enzymes involved in the posttranslational processing of their encoded proteins (p21s) attractive targets for the development of new drugs. Although most effort has focused on farnesyl transferase, which catalyzes the first processing step, attachment of palmitate to p21 is required for optimal transformation by H-ras and N-ras. We have demonstrated that the natural product cerulenin ([2R,3S]-2,3-epoxy-4-oxo-7,10-trans,trans-dodecadienamide) inhibits the palmitoylation of H-ras-and N-ras-encoded p21s in parallel with inhibition of cell proliferation. More than 30 analogues of cerulenin, both aromatic and aliphatic, with various chain lengths and amide substitutions, have been synthesized for use in SAR studies. Studies on the inhibition of T24 cell proliferation indicate that the α-keto-epoxy moiety is critical for cytotoxicity, while alkyl chain length had only modest effects on potency. Several compounds inhibited the incorporation of [3H]palmitate into p21 in intact T24 cells, with the unsubstituted carboxamides being more active than N,N-dimethyl compounds. In contrast to the effects on palmitoylation, the only compounds which inhibited fatty acid synthase contained alkyl side chains of 12 carbons or fewer. Regression analyses indicated that inhibition of palmitoylation is more closely related to inhibition of proliferation than is inhibition of fatty acid synthase. Further characterization of the molecular pharmacology of these and analogous compounds may define a new class of drugs with antitumor activity.

PdII-catalyzed oxidative dimeric cyclization-coupling reaction of 2,3-allenoic acids: an efficient synthesis of bibutenolide derivatives

Ma, Shengming,Yu, Zhanqian,Gu, Zhenhua

, p. 2351 - 2356 (2005)

Three sets of convenient catalytic systems have been developed for the oxidalive dimeric cyclization coupling of differently substituted 2,3-allenoic acids catalyzed by PdII, affording bibutenolides that are not otherwise readily available. The advantages and disadvantages of these systems are discussed. Although the diastereoselectivity for the bicyclization of racemic 2,3-allenoic acids is low, excellent diastereoselectivity was realized in the bicyclization reaction of optically active 23-allenoic acids, leading to the optically active bibutenolides in high yields and ee. Based on a mechanistic study, it is believed that the reaction may proceed by means of a double oxypalladation and reductive elimination to yield butenolide 3 and Pd° species, which may be reoxidized to the catalytically active PdII species in the presence of alkyl iodide/air, metallic iodide/air, or benzoquinone.

A facile synthesis of γ-butenolides via cyclization of 3-alkenoic acids with dimethyl sulfoxide and oxalyl bromide

Ding, Rui,Liu, Yongguo,Liu, Lei,Li, Huimin,Tao, Sichen,Sun, Baoguo,Tian, Hongyu

, p. 3001 - 3007 (2019)

The combination of dimethyl sulfoxide and oxalyl bromide was used to accomplish the cyclization of 3-alkenoic acids with the aid of a base to afford γ-butenolides, in which bromodimethylsulfonium salt generated in situ was proposed to serve as a Br+ source.

Lewis base-catalyzed electrophilic lactonization of selenyl bromide resin and facile solid-phase synthesis of furan-2(5H)-one derivatives

Jun He, Rong,Chun Zhu, Bing,Wang, Yu Guang

, p. 523 - 528 (2014/07/07)

A facile solid-phase synthesis approach was developed for the rapid synthesis of multi-substituted furan-2(5H)-one derivatives libraries. The synthetic strategy included the selenyl bromide resin-induced electrophilic lactonization catalyzed by Lewis base, lithiation, nucleophilic substitution and oxidation-elimination of the selenium resins. The advantages of the new method are good yields, high purity, straightforward operations and high diversity of the products, lack of odor, and good stability of the selenium resins. Copyright

Cerulenin analogues as inhibitors of efflux pumps in drug-resistant candida albicans

Diwischek, Florian,Morschhae, Joachim,Holzgrabe, Ulrike

experimental part, p. 150 - 164 (2009/05/07)

Overexpression of the ABC transporters Cdrl and Cdr2 or the major facilitator Mdrl causes multidrug resistance in the human fungal pathogen Candida albicans. The fatty acid synthesis inhibitor cerulenin and the structurally unrelated Golgi transport inhibitor brefeldin A are substrates for both types of efflux pumps in Candida albicans. In an effort to overcome efflux pump-mediated drug resistance in Candida albicans, cerulenin analogues were generated using a variety of synthesis pathways. The so obtained cerulenin derivatives were tested on multidrug-resistant Candida albicans isolates which constitutively overexpress either Mdr1 or Cdr1 and Cdr2. Some of these compounds were found to decrease Mdr1-mediated resistance to brefeldin A up to eight-fold compared to the control. 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Photochemical reactions of chromium-alkoxycarbene complexes with stabilized ylides to produce "push-pull" captodative allenes

Sestrick, Michael R.,Miller, Michael,Hegedus, Louis S.

, p. 4079 - 4088 (2007/10/02)

Photolysis of chromium alkoxycarbene complexes in the presence of stabilized ylides produced allenes having electron withdrawing groups on C-1 and electron donating groups on C-3. These highly reactive captodative allenes rearranged to 1,3-substituted-1,3-dienes under mildly acidic conditions and hydrolyzed to γ-keto-α,β-unsaturated esters, both in excellent yield.

Nitrodienic-like Reactivity of 2-Nitrofuran with Organometallic Reagents: One-step Synthesis of Alkylfuranones

Pecunioso, Angelo,Galoppini, Elena,Menicagli, Rita

, p. 7497 - 7508 (2007/10/02)

2-Nitrofuran reacts with Grignard, alkyllithium, dialkylcadmium and heterocuprate reagents affording mixtures of 5-alkyl- and 3-alkyl-2-furanones.

ALKYLFURANONES FROM 2-NITROFURAN: A PROMISING SYNTHETIC APPROACH

Menicagli, Rita,Pecunioso, Angelo,Galoppini, Elena

, p. 141 - 142 (2007/10/02)

Mixtures of 5- and 3-alkyl-2-furanones are obtained from 2-nitrofuran and Grignard reagents.

Manganese(III) γ-Lactone Annulation with Substituted Acids

Fristad, William E.,Peterson, John R.,Ernst, Andreas B.

, p. 3143 - 3148 (2007/10/02)

Manganese(III) acetate oxidation of several HOOCCH2X, X = electron withdrawing group, in the presence of alkenes led to the formation of α-substituted γ-lactones.Chloroacetic acid gave α-chloro-γ-lactones, which were converted in two steps to the corresponding α,β-unsaturated γ-lactones. 3-Chloropropanoic acid led to the α-methylene γ-lactone after base induced elimination of HCl.Cyanoacetic acid produced α-cyano γ-lactones which could be hydrolytically decyanated or converted to the α-methylene γ-lactones in two steps.Potassium methyl malonate was oxidized and annulated onto alkenes to give α-carbomethoxy γ-lactones in reasonable yields.The method demonstrates a general route into several useful types substituted γ-lactones.

NOUVELLE METHODE DE SYNTHESE DES γ-LACTONES ET (5H)FURANNONES-2-MONOSUBSTITUEES

Canonne, P.,Akssira, M.

, p. 3453 - 3456 (2007/10/02)

3-monosubstituted γ-lactones and 5-mono- or 3,5-disubstituted 2-(5-H)-furanones have been prepared by the reaction of Grignard reagents with lactols.

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