ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME

Product Name
ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME
CAS No.
22472-58-8
Chemical Name
ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME
Synonyms
ISONITROSO-D-CAMPHOR;camphorquinone 3-oxime;(1R,E)-(+)-CAMPHORQUINONE 3-OXIME;(1R,E)-(+)-2,3-BORNANEDIONE 3-OXIME;ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME;ANTI-(1R)-(+)-2,3-BORNANEDIONE 3-OXIME
CBNumber
CB4476401
Molecular Formula
C10H15NO2
Formula Weight
181.23
MOL File
22472-58-8.mol
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ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME Property

Melting point:
153-156 °C(lit.)
storage temp. 
2-8°C
solubility 
soluble in DCM, Ethyl Acetate, Ether, Methanol
form 
Solid
color 
Pale Yellow
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Safety

Safety Statements 
22-24/25
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
C175005
Product name
(1R,4S)-CamphorquinoneMonooxime
Packaging
10g
Price
$820
Updated
2021/12/16
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ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME Chemical Properties,Usage,Production

Uses

(1R,4S)-Camphorquinone Monooximeis an intermediate in the synthesis of Gibornuride (G409700), an anti-diabetic drug from the group of sulfonylureas.

ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME Preparation Products And Raw materials

Raw materials

Preparation Products

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ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME Suppliers

CHINA 2 India 1 United States 1 Global 4
Riedel-de Haen AG
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Country
United States
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22472-58-8, ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIMERelated Search:

(1R)-(-)-CAMPHORQUINONE ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME DL-Camphor 4-METHYL-2-PENTANONE OXIME isobutyraldehyde oxime Cyclohexanone oxime heptanal oxime 2-Octanone oxime 5-METHYL-3-HEPTANONE OXIME CYCLOPENTANONE OXIME 5-METHYL-2-HEXANONE OXIME 2,4-DIMETHYLCYCLOPENTANONE ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME 2-HEPTANONE OXIME 2-METHYLVALERALDEHYDE OXIME

  • ISONITROSO-D-CAMPHOR
  • ANTI-(1R)-(+)-2,3-BORNANEDIONE 3-OXIME
  • ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME
  • (1R,E)-(+)-2,3-BORNANEDIONE 3-OXIME
  • (1R,E)-(+)-CAMPHORQUINONE 3-OXIME
  • camphorquinone 3-oxime
  • 22472-58-8
  • Organic Building Blocks
  • Oximes
  • Chiral Building Blocks
  • Asymmetric Synthesis
  • Terpenes
  • Bicyclic Monoterpenes