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Catalog Number:
39149
CAS Number:
10293-06-8
+)-3-Bromocamphor
Purity:
≥ 98% (GC)
Synonym(s):
(+)-Camphor bromide, endo-(1R-3-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one, endo-(1R)-3-Bromocamphor
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Product Information

(+)-3-Bromocamphor is a versatile organic compound known for its unique properties and applications in various fields. This chiral brominated camphor derivative is primarily utilized in the synthesis of pharmaceuticals and agrochemicals, where its structural characteristics can enhance biological activity. Researchers appreciate its role as a chiral building block in asymmetric synthesis, allowing for the development of enantiomerically pure compounds that are crucial in drug formulation. Additionally, (+)-3-Bromocamphor serves as a valuable intermediate in the production of fragrances and flavoring agents, contributing to the formulation of complex aromatic profiles.

The compound's distinctive bicyclic structure not only imparts stability but also facilitates its use in the development of novel materials and catalysts. Its applications extend to the field of organic synthesis, where it can be employed in various reactions, including nucleophilic substitutions and cycloadditions. With its proven efficacy and adaptability, (+)-3-Bromocamphor stands out as an essential compound for researchers and industry professionals seeking innovative solutions in chemical synthesis and product development.

Synonyms
(+)-Camphor bromide, endo-(1R-3-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one, endo-(1R)-3-Bromocamphor
CAS Number
10293-06-8
Purity
≥ 98% (GC)
Molecular Formula
C10H15BrO
Molecular Weight
231.13
MDL Number
MFCD00003744
PubChem ID
6438
Melting Point
75 - 77 °C
Appearance
White to off-white crystalline powder
Boiling Point
274 °C
Optical Rotation
[α]20D = 130 - 145 ° (C = 2 in EtOH)
Conditions
Store at RT
General Information
Synonyms
(+)-Camphor bromide, endo-(1R-3-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one, endo-(1R)-3-Bromocamphor
CAS Number
10293-06-8
Purity
≥ 98% (GC)
Molecular Formula
C10H15BrO
Molecular Weight
231.13
MDL Number
MFCD00003744
PubChem ID
6438
Melting Point
75 - 77 °C
Appearance
White to off-white crystalline powder
Boiling Point
274 °C
Optical Rotation
[α]20D = 130 - 145 ° (C = 2 in EtOH)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(+)-3-Bromocamphor is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, allowing researchers to create complex molecules efficiently.
  • Chiral Auxiliary: It is used as a chiral auxiliary in asymmetric synthesis, helping to produce enantiomerically pure compounds, which are crucial in pharmaceuticals.
  • Pharmaceutical Applications: The compound is explored for its potential therapeutic effects, particularly in the development of new drugs targeting various health conditions.
  • Flavor and Fragrance Industry: Its unique scent profile makes it valuable in the formulation of fragrances and flavorings, enhancing product appeal in cosmetics and food.
  • Research in Material Science: (+)-3-Bromocamphor is investigated for its properties in creating novel materials, including polymers with specific characteristics for industrial applications.

Citations