16346-63-7

Basic information

• Product Name: (1S,4S)-Norborna-5-ene-2-one
• Synonyms: (-)-Dehydronorcamphor;(1S,4S)-Bicyclo[2.2.1]hepta-2-ene-6-one;(1S,4S)-Bicyclo[2.2.1]hepta-5-ene-2-one;(1S,4S)-Norborna-5-ene-2-one;[1S,4S,(-)]-Bicyclo[2.2.1]hept-5-en-2-one;[1S,4S,(-)]-Bicyclo[2.2.1]hepta-5-ene-2-one;(1β,4β)-Bicyclo[2.2.1]hepta-5-ene-2-one;[1R,4R,(+)]-Bicyclo[2.2.1]hept-5-en-2-one
• CAS NO: 16346-63-7
• Molecular Formula: C₇H₈O
• Molecular Weight: 108.14
• Mol File: 16346-63-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 70-80 °C(Press: 20 Torr)
• Appearance: /
• Density: 1.138±0.06 g/cm3(Predicted)
• CAS DataBase Reference: (1S,4S)-Norborna-5-ene-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,4S)-Norborna-5-ene-2-one(16346-63-7)
• EPA Substance Registry System: (1S,4S)-Norborna-5-ene-2-one(16346-63-7)

Safety Data

• Hazardous Substances Data: 16346-63-7(Hazardous Substances Data)

Usage

General Description

(1S,4S)-Norborna-5-ene-2-one is a bicyclic organic compound with a norbornane backbone and a ketone functional group. It is also known as endo-(+)-5-norbornene-2-one. (1S,4S)-Norborna-5-ene-2-one is a colorless liquid with a camphor-like odor and is commonly used as a flavor and fragrance agent. It is also a building block in the synthesis of various pharmaceuticals and agricultural chemicals. The unique structure of (1S,4S)-Norborna-5-ene-2-one makes it a versatile intermediate in organic synthesis, and it is used in the production of polymers, resins, and other industrial chemicals.

Upstream product

• 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 
• 694-98-4 norborn-5-en-2-one 
• 83759-48-2 C₁₁H₁₆O₂ 
• 83759-48-2 C₁₁H₁₆O₂ 

Downstream Products

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

Relevant articles and documents

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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.