10293-09-1

Basic information

• Product Name: (1R,4R,7R)-9-bromocamphor
• Synonyms: (1R,4R,7R)-9-bromocamphor
• CAS NO: 10293-09-1
• Molecular Weight: 231.132
• Mol File: 10293-09-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1R,4R,7R)-9-bromocamphor(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,4R,7R)-9-bromocamphor(10293-09-1)
• EPA Substance Registry System: (1R,4R,7R)-9-bromocamphor(10293-09-1)

Safety Data

• Hazardous Substances Data: 10293-09-1(Hazardous Substances Data)

Upstream product

• 85706-52-1 (+)-endo-3,9,10-tribromocamphor 
• 91-22-5 quinoline 
• 24393-70-2 isoborneol 
• 464-49-3 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 10293-10-4 dibromocamphor 
• 10293-10-4 rac-3,9-dibromocamphor 
• 76-29-9 3-bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 

Downstream Products

• 96837-64-8 Toluene-4-sulfonic acid 3-((1R,3S,4R,7R)-2-hydroxy-1,3,7-trimethyl-bicyclo[2.2.1]hept-7-yl)-propyl ester 
• 96837-65-9 Toluene-4-sulfonic acid 3-[(1R,5R)-1,2-dimethyl-5-((S)-1-methyl-2-oxo-ethyl)-cyclopent-2-enyl]-propyl ester 
• 6248-95-9 1,7-<¹⁴C2>-Dimethyl-2-oxo-norbornan-7anti-carbonsaeure 
• 103386-85-2 (1S)-3a,6a-dimethyl-hexahydro-1,5-cyclo-pentalen-4-one 
• 111013-51-5 C₁₇H₂₂⁽²⁾HNO 
• 10334-10-8 rac-9-hydroxyisoborneol 
• 10334-10-8 rac-9-hydroxyborneol 
• 6248-95-9 rac-trans-isoketopinic acid 
• 122763-78-4 Acetic acid (R)-[(1S,6R)-2-(diethoxy-phosphoryloxy)-6-isopropenyl-3-methyl-cyclohex-2-enyl]-furan-2-yl-methyl ester 
• 122763-79-5 2-((1S,6R)-6-Isopropenyl-3-methyl-cyclohex-2-enylmethyl)-furan 
• 5989-27-5 D-limonene 
• 187241-52-7 (1R,2R,4R,7R)-7-(Diphenyl-phosphinoylmethyl)-1,7-dimethyl-bicyclo[2.2.1]heptan-2-ol 
• 187241-51-6 (1R,4R,7R)-7-(Diphenyl-phosphinoylmethyl)-1,7-dimethyl-bicyclo[2.2.1]heptan-2-one 
• 218271-70-6 Benzoic acid (1S,2R,3R)-2-benzyloxycarbonyl-3-hydroxymethyl-2,3-dimethyl-cyclopentylmethyl ester 

Relevant articles and documents

Constituents of the essential oil of Strobilanthes auriculatus

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Ring cleavage of camphor derivatives: formation of chiral synthons for natural products synthesis

Base-promoted ring cleavage of 9,10- and 8,10-dibromocamphor provides chiral intermediates for natural product synthesis.