16346-63-7

Usage

Uses

Used in Flavor and Fragrance Industry:
(1S,4S)-Norborna-5-ene-2-one is used as a flavor and fragrance agent due to its distinctive camphor-like odor.
Used in Pharmaceutical Industry:
(1S,4S)-Norborna-5-ene-2-one is used as a building block in the synthesis of various pharmaceuticals, contributing to the development of new medications.
Used in Agricultural Chemical Industry:
(1S,4S)-Norborna-5-ene-2-one is used in the synthesis of agricultural chemicals, playing a role in the production of pesticides and other agrochemicals.
Used in Polymer and Resin Production:
(1S,4S)-Norborna-5-ene-2-one is used as an intermediate in the production of polymers and resins, which are essential in various industrial applications.
Used in Organic Synthesis:
The unique structure of (1S,4S)-Norborna-5-ene-2-one makes it a versatile intermediate in organic synthesis, utilized in the creation of a wide range of industrial chemicals.

Upstream product

• 83759-48-2 C₁₁H₁₆O₂ 
• 83759-48-2 C₁₁H₁₆O₂ 
• 694-98-4 norborn-5-en-2-one 
• 2564-83-2 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical 
• 96443-41-3 (1R,2S,4R)-bicyclo[2.2.1]hept-5-ene-2-carbaldehyde 

Downstream Products

• 83759-48-2 C₁₁H₁₆O₂ 
• 497-38-1 (1S,4R)-bicyclo[2.2.1]heptan-2-one 
• 16187-25-0 2-phenylbicyclo<2.2.1>hept-5-en-2endo-ol 
• 802911-54-2 ethyl (1R,2R,3R,4R,5R)-6-oxotricyclo[3.2.1.0^2,4]octane-3-carboxylate 
• 802911-57-5 ethyl (1R,2R,3S,4R,5R)-6-oxotricyclo[3.2.1.0^2,4]octane-3-carboxylate 
• 133149-20-9 C-((1R,2R)-2-Benzyloxy-cyclopent-3-enyl)-methylamine 
• 133149-19-6 ((1R,2S)-2-Benzyloxy-cyclopent-3-enyl)-acetic acid 
• 133149-21-0 Acetic acid (1R,2R)-2-benzyloxy-cyclopent-3-enylmethyl ester 
• 133149-22-1 Acetic acid (1S,2S,3R,5S)-2-benzyloxy-6-oxa-bicyclo[3.1.0]hex-3-ylmethyl ester 
• 133149-23-2 Acetic acid (1R,2S,3S,4R)-2-benzyloxy-3-hydroxy-4-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-cyclopentylmethyl ester 
• 133268-28-7 N-[9-((1R,2S,3S,4R)-2,3-Dihydroxy-4-hydroxymethyl-cyclopentyl)-9H-purin-6-yl]-benzamide 
• 133149-24-3 Acetic acid (1R,2S,3S,4R)-4-(6-benzoylamino-purin-9-yl)-2-benzyloxy-3-hydroxy-cyclopentylmethyl ester 
• 38397-34-1 (1S)-2-norbornenone tosylhydrazone 
• 83759-48-2 C₁₁H₁₆O₂ 

Relevant academic research and scientific papers

Oxidative C-C bond cleavage of aldehydes via visible-light photoredox catalysis

The visible-light mediated oxidative C-C bond cleavage of aldehydes has been achieved in good yields at ambient temperature and open to air using Ru(bpy)3Cl2 (bpy = 2,2′-bipyridine) as the photoredox catalyst. Moreover, we further demonstrated the application in a tandem Michael/oxidative C-C bond cleavage reaction.

Bacillus stearothermophilus alcohol dehydrogenase: A new catalyst to obtain enantiomerically pure bicyclic octen- and hepten-ols and -ones

From the cells of Bacillus stearothermophilus a new enzyme has been isolated, which catalyses the stereospecific redox reactions of bicyclic octen- and hepten- ols and -ones.

DETERMINATION DE PURETE ENANTIOMERIQUE PAR RMN13C DANS LES SERIES DES BICYCLO(2.2.1.)-HEPTANE ET BICYCLO(2.2.1.)-HEPTENE

N.M.R.13C peak assignments were established for each diastereoisomeric ketal form of norbornanone (+/-), or norbornenone (+/-).This method offers an attractive route for the determination of the optical purity of these ketones.