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Catalog Number:
24609
CAS Number:
39637-74-6
(1S)-(-)-Camphanic chloride
Purity:
≥ 99% (GC)
Synonym(s):
(-)-Camphanoyl chloride, (1S)-3-Oxo-4,7,7-trimethyl-2-oxabicyclo[2.2.1]heptane-1-carbonyl chloride
Hazmat
Documents
$36.65 /1G
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Product Information
Synonyms
(-)-Camphanoyl chloride, (1S)-3-Oxo-4,7,7-trimethyl-2-oxabicyclo[2.2.1]heptane-1-carbonyl chloride
CAS Number
39637-74-6
Purity
≥ 99% (GC)
Molecular Formula
C10H13ClO3
Molecular Weight
0
MDL Number
MFCD00135626
PubChem ID
558230
Melting Point
68 - 71 °C
Appearance
White to grey white crystallization
Optical Rotation
[a]D25 = -24.7 ± 1 ° (C=3.57 CHCl3)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
(-)-Camphanoyl chloride, (1S)-3-Oxo-4,7,7-trimethyl-2-oxabicyclo[2.2.1]heptane-1-carbonyl chloride
CAS Number
39637-74-6
Purity
≥ 99% (GC)
Molecular Formula
C10H13ClO3
Molecular Weight
0
MDL Number
MFCD00135626
PubChem ID
558230
Melting Point
68 - 71 °C
Appearance
White to grey white crystallization
Optical Rotation
[a]D25 = -24.7 ± 1 ° (C=3.57 CHCl3)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(1S)-(-)-Camphanic chloride is widely utilized in research focused on

  • Synthesis of Pharmaceuticals: This compound serves as an important intermediate in the synthesis of various pharmaceutical agents, particularly in the development of analgesics and anti-inflammatory drugs.
  • Flavor and Fragrance Industry: It is used to create specific flavor profiles and fragrances, providing a unique scent and taste that enhances food products and perfumes.
  • Organic Synthesis: Researchers employ it in organic synthesis reactions, particularly in the formation of complex organic molecules, due to its reactive nature and ability to introduce functional groups.
  • Chiral Auxiliary: As a chiral compound, it is utilized in asymmetric synthesis, helping chemists produce enantiomerically pure compounds, which is crucial in drug development.
  • Research in Chemical Biology: It is used in studies involving enzyme catalysis and biomolecular interactions, aiding researchers in understanding biological processes at the molecular level.

Citations