100818-77-7

Usage

Uses

Used in Organic Synthesis:
(S)-5-Benzyloxy-6-oxo-hexanenitrile is used as a building block for constructing more complex molecules in the field of organic synthesis. Its versatile nature and utility in various chemical reactions contribute to its importance in this industry.
Used in Medicinal Chemistry:
In the pharmaceutical sector, (S)-5-Benzyloxy-6-oxo-hexanenitrile is utilized as a building block for the development of new pharmaceuticals. Its unique structure allows for the creation of molecules with specific therapeutic properties.
Used in Agrochemicals:
(S)-5-Benzyloxy-6-oxo-hexanenitrile is also employed in the agrochemical industry as a key intermediate in the synthesis of various agrochemical products, contributing to its significance in this field.
Used in Fine Chemicals:
(S)-5-Benzyloxy-6-oxo-hexanenitrile is used as an intermediate in the production of fine chemicals, which are high-purity chemicals used in various applications, including the fragrance, flavor, and specialty chemical industries.
Used as a Chiral Building Block:
(S)-5-Benzyloxy-6-oxo-hexanenitrile is used as a chiral building block in the synthesis of optically active compounds. Its ability to create enantiomerically pure molecules is highly valuable in the development of single-enantiomer drugs, which can have significant advantages in terms of efficacy and safety.

Upstream product

• 79364-35-5 (S)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)but-3-en-1-ol 
• 100818-75-5 Methanesulfonic acid (S)-4-benzyloxy-4-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-butyl ester 
• 100-39-0 benzyl bromide 
• 100818-74-4 2,3-dideoxy-5,6-O-(1-methylethylidene)-4-O-bnezyl-D-erythro-hexitol 
• 87604-53-3 (R)-4-((S)-1-(benzyloxy)but-3-ene-1-yl)-2,2-dimethyl-1,3-dioxypentane 
• 100818-76-6 (5S,6R)-5-(benzyloxy)-6,7-dihydroxyheptanenitrile 6,7-acetonitrile 
• 132047-76-8 (5S,6R)-5-Benzyloxy-6,7-dihydroxy-heptanenitrile 

Downstream Products

• 100818-78-8 (E)-(S)-5-Benzyloxy-8-oxo-oct-6-enenitrile 
• 100843-81-0 (Z)-(S)-5-Benzyloxy-7-bromo-8-oxo-oct-6-enenitrile 
• 132047-84-8 (1R,2R,4aS,5S,8aR)-5-Benzyloxy-2-(3-hydroxy-propyl)-1-methyl-1,2,4a,5,6,7,8,8a-octahydro-naphthalene-1-carboxylic acid methyl ester 
• 100818-84-6 methyl 1α-(benzyloxy)-6β-(3'-hydroxyprop-2'-en-1'-yl)-5α-methyl-1,2,3,4,4aβ,5,6,8aα-octahydronaphthalene-5β-carboxylate 
• 100818-81-3 methyl (2E,7S,8Z,10E,12E)-7-(benzyloxy)-9-bromo-14-hydroxy-2-methyltetradeca-2,7,8,20-tetraenoate 
• 100818-80-2 (2E,4E,6Z)-(S)-8-Benzyloxy-6-bromo-11-cyano-undeca-2,4,6-trienoic acid ethyl ester 
• 100818-82-4 methyl 1α-(benzyloxy)-8-bromo-6β-(3'-hydroxyprop-2'-en-1'-yl)-5α-methyl-1,2,3,4aβ,5,6,8aα-octahydronaphthalene-5β-carboxylate 
• 100818-83-5 methyl 1α-(benzyloxy)-8-bromo-6β-(3'-hydroxy-prop-2'-en-1'-yl)-5β-methyl-1,2,3,4aα,5,6,8aα-octahydronaphthalene-5α-carboxylate 
• 132047-80-4 (6Z,8E,10E)-(S)-5-Benzyloxy-7-bromo-12-hydroxy-dodeca-6,8,10-trienal 
• 132047-78-0 (6Z,8E)-(S)-5-Benzyloxy-7-bromo-10-hydroxy-deca-6,8-dienal 
• 132047-85-9 (1R,2S,4aS,5S,8aR)-5-Benzyloxy-2-(3-hydroxy-propyl)-1-methyl-decahydro-naphthalene-1-carboxylic acid methyl ester 
• 132047-77-9 (2E,4Z)-(S)-6-Benzyloxy-4-bromo-9-cyano-nona-2,4-dienoic acid methyl ester 
• 100818-87-9 methyl (2E,7S,8Z,10E)-7-(benzyloxy)-9-bromo-12-hydroxydodeca-2,8,10-trienoate 
• 132047-79-1 methyl (2E,7S,8Z,10E)-7-(benzyloxy)-9-bromo-12-hydroxy-2-methyldodeca-2,8,10-trienoate 

Relevant academic research and scientific papers

Enantioselective Synthesis of the Bottom Half of Chlorothricolide. 3. Studies of the Steric Directing Group Strategy for Stereocontrol in Intramolecular Diels-Alder Reactions

The intramolecular Diels-Alder reactions of a series of C(7)-alkoxy-substituted 2(E),8(Z),10(E)-undecatrienoates and trienals containing removable C(9)-Br or C(9)-SiMe3 substituents (11, 12, 13, 33, 42, 43, 44, 45) were studied as part of a programm direc

Enantioselective synthesis of the bottom-half of chlorothricolide

The first enantioselective synthesis of a chlorothricolide intermediate is described. The synthesis features the intramolecular Diels-Alder reaction of tetraene.