1577-31-7

Usage

Uses

Used in the Fragrance Industry:
(Z)-2-Heptenoic acid is utilized as a flavoring agent in food and beverages, capitalizing on its natural fruity scent to enhance the aroma and taste of various products.
Used in the Production of Synthetic Perfumes:
(Z)-2-Heptenoic acid serves as a key ingredient in the creation of synthetic perfumes, where its unique odor profile contributes to the development of complex and appealing fragrances.
Used as a Precursor in Chemical Synthesis:
(Z)-2-Heptenoic acid is employed as a precursor for the synthesis of other chemical compounds, highlighting its versatility and importance in the realm of organic chemistry.
Used in Antimicrobial Formulations:
Leveraging its antimicrobial properties, (Z)-2-Heptenoic acid is incorporated into the development of antimicrobial agents, playing a crucial role in combating microbial growth and maintaining hygiene.
Used in the Pharmaceutical Industry:
Due to its biological and pharmacological activities, (Z)-2-Heptenoic acid holds potential applications within the pharmaceutical sector, where it may contribute to the development of new drugs and therapies.

InChI:InChI=1/C7H12O2/c1-2-3-4-5-6-7(8)9/h5-6H,2-4H2,1H3,(H,8,9)/b6-5-

Upstream product

• 1483-67-6 hept-2-ynoic acid 
• 124-38-9 carbon dioxide 
• 109-72-8 n-butyllithium 
• 74-86-2 acetylene 
• 16930-95-3 ethyl hept-2-ynoate 
• 693-02-7 hex-1-yne 
• 35066-42-3 ethyl (Z)-hept-2-enoate 
• 13154-12-6 (Z)-1-bromohex-1-ene 
• 1577-30-6 1,3-Dibrom-2-heptanon 
• 54340-72-6 ethyl (E)-2-heptenoate 
• 624-20-4 1,2-dibromohexane 

Downstream Products

• 51193-77-2 (Z)-oct-3-en-2-one 
• 13154-12-6 1-bromohexene 

Relevant academic research and scientific papers

Influence of the double-bond geometry of the Michael acceptor on copper-catalyzed asymmetric conjugate addition

Focusing on mechanistic aspects, a study of the influence of the (E)/(Z) double-bond geometry of the Michael acceptor on the enantioselectivity of copper-catalyzed asymmetric conjugate addition reactions has been realized. In spite of numerous articles co

Carbamoyl substituted heterocycles

This invention relates to carbamoyl substituted heterocycles which are ω-phenyl-ω-(3-pyridyl)-ω-alkenoic acid derivatives bearing a carbamoyl substituted oxazolyl or oxazolinyl group on the phenyl ring and which demonstrate utility for thromboxane receptor antagonism and/or thromboxane synthase inhibition, as well as pharmaceutical formulations containing them, methods for their use, and processes and intermediates for their preparation.

PREPARATION OF SUBSTITUTED ALKENOIC ACIDS

This invention relates to a highly selective process for preparation of E-ω-phenyl-ω-(3-pyridyl)-ω-alkenoic acid derivatives bearing a carbamoyl substituted oxazolyl or oxazolinyl group on the phenyl ring which demonstrate utility for thromboxane receptor antagonism and/or thromboxane synthase inhibition, as well as to intermediates therefor.

Carbamoyl substituted oxazoles as thromboxane receptor antagonists

This invention relates to carbamoyl substituted heterocycles which are ω-phenyl-ω-(3-pyridyl)-ω-alkenoic acid derivatives bearing a carbamoyl substituted oxazolyl or oxazolinyl group on the phenyl ring and which demonstrate utility for thromboxane receptor antagonism and/or thromboxane synthase inhibition, as well as pharmaceutical formulations containing them, methods for their use, and processes and intermediates for their preparation.

Vinyl-copper derivatives-XI1 1 Part X: A. Alexakis, G. Cahiez and J.F. Normant, Synthesis, 826 (1979). Reactivity of Z-alkenyl cuprates towards various electrophiles. Application to the synthesis of some natural products

Z-Alkenylcuprates 1 and 2, prepared in situ by addition of acetylene to alkylcuprates, react with a variety of electrophiles (epoxides, carbon dioxide, aldehydes) and give conjugate addition products with α,β-unsaturated aldehydes, ketones and esters, and with activated cyclopropanes. They also add across the triple bond of some alkynes. The synthesis of natural products (7,9,22) is described.