14017-81-3 Usage
Description
4-Hexenoic acid, methyl ester, (4E)is a chemical compound characterized by the molecular formula C8H14O2. Commonly referred to as hex-4-enoic acid methyl ester, this compound exhibits a slightly fruity and floral scent. It is recognized for its versatile applications across different industries due to its distinct aromatic properties and chemical structure.
Uses
Used in the Food Industry:
4-Hexenoic acid, methyl ester, (4E)is utilized as a flavoring agent, specifically in the creation of fruit and berry flavors. Its natural aroma profile contributes to enhancing the taste and olfactory experience of various food products.
Used in the Fragrance Industry:
In the realm of perfumery and scented products, 4-Hexenoic acid, methyl ester, (4E)is employed for its sweet and fruity aroma. It is incorporated into perfumes, colognes, and other fragrances to provide a pleasant and complex scent profile.
Used in the Pharmaceutical Industry:
4-Hexenoic acid, methyl ester, (4E)also holds potential in the pharmaceutical sector as a building block for the synthesis of a range of drugs and pharmaceutical compounds. Its chemical properties make it a valuable precursor in the development of new medications and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 14017-81-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,1 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14017-81:
(7*1)+(6*4)+(5*0)+(4*1)+(3*7)+(2*8)+(1*1)=73
73 % 10 = 3
So 14017-81-3 is a valid CAS Registry Number.
14017-81-3Relevant articles and documents
Tandem RCM of Dienynes for the Construction of Taxol-Type Carbocyclic Systems
Garcia-Fandino, Rebeca,Codesido, Eva M.,Sobarzo-Sanchez, Eduardo,Castedo, Luis,Granja, Juan R.
, p. 193 - 196 (2007/10/03)
(Matrix presented) Tandem ring-closing metathesis of hydrindanone dienynes allows access to taxosteroids, a new class of compounds that combine the [5.3.1] carbocyclic system of taxanes with rings C and D of the steroid skeleton.
Lithium/Ammonia Reductions of 2-Thiophenecarboxylic Acids
Blenderman, Walter G.,Joullie, Madeleine M.,Preti, George
, p. 3206 - 3213 (2007/10/02)
Lithium/ammonia reductions of 2-thiophenecarboxylic acids (1) in the absence of a proton source afforded mixtures of products.In the presence of methanol acyclic mercapto carboxylic acids (4) were the major products.Ring closure of 4 to the corresponding thiolactones (12) showed the double bonds in 4 to be of cis geometry.Attempts were made to prepare Z olefinic compounds derived from these mercapto carboxylic acids.Lithium 2-thiophenecarboxylate salts (2) afforded good yields of the corresponding 2,5-dihydro-2-thiophenecarboxylic acids (3).The presence of substituents on the ring and the ratio of metal to acid were significant factors in determining the nature of this products.A mechanism is proposed to explain the products observed.