ChemicalBook > CAS DataBase List > ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME

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

Product Name
ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME
CAS No.
31571-14-9
Chemical Name
ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME
Synonyms
(1R,4S,E);-3-(Hydroxyimino);ISONITROSO-D-CAMPHOR;(1R,E)-(+)-CAMPHORQUINONE 3-OXIME;(1R,E)-(+)-2,3-BORNANEDIONE 3-OXIME;ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME;ANTI-(1R)-(+)-2,3-BORNANEDIONE 3-OXIME;anti-(1R)-(+)-Camphorquinone 3-Oxime >ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME, 99 %;(1R,E)-(+)-2,3-Bornanedione 3-oxime, anti-(1R
CBNumber
CB7476402
Molecular Formula
C10H15NO2
Formula Weight
181.23
MOL File
31571-14-9.mol
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ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME Property

Melting point:
153-156 °C(lit.)
Boiling point:
276.8±7.0 °C(Predicted)
Density 
1.25±0.1 g/cm3(Predicted)
refractive index 
196 ° (C=1, EtOH)
storage temp. 
2-8°C
pka
9.35±0.60(Predicted)
form 
powder to crystal
color 
White to Orange to Green
optical activity
[α]25/D +200°, c = 1 in ethanol
Sensitive 
Air Sensitive
BRN 
3200377
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Safety

Safety Statements 
22-24/25
WGK Germany 
3
HS Code 
2928.00.5000
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
273112
Product name
(1R,E)-(+)-Camphorquinone 3-oxime
Purity
99%
Packaging
1g
Price
$232
Updated
2023/06/20
TCI Chemical
Product number
C1661
Product name
anti-(1R)-(+)-Camphorquinone 3-Oxime
Purity
>95.0%(GC)(N)
Packaging
1g
Price
$121
Updated
2024/03/01
Alfa Aesar
Product number
H51034
Product name
(1R,E)-(+)-Camphorquinone 3-oxime, 99%
Packaging
5g
Price
$473
Updated
2023/06/20
Alfa Aesar
Product number
H51034
Product name
(1R,E)-(+)-Camphorquinone 3-oxime, 99%
Packaging
1g
Price
$118
Updated
2021/12/16
TRC
Product number
C175015
Product name
anti-(1R)-(+)-Camphorquinone 3-Oxime
Packaging
100mg
Price
$90
Updated
2021/12/16
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ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME Chemical Properties,Usage,Production

Uses

(1R,E)-(+)-Camphorquinone 3-oxime can be used to prepare chiral camphor-oxazoline auxiliary, which is used to blend diastereoselectivity and isomer separability for the efficient synthesis of bicuculline, egenine, corlumine, and corytensine.

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

Raw materials

Preparation Products

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

Americas 1 China 32 Europe 1 Germany 1 India 2 Japan 1 Switzerland 1 United Kingdom 1 United States 4 Global 44
TCI AMERICA
Tel
800-4238616
Fax
+1-888-520-1075 / +1-503-283-1987
Email
sales@tciamerica.com
Country
Americas
ProdList
23653
Advantage
75

31571-14-9, ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIMERelated Search:

DL-CAMPHORIC ANHYDRIDE (+/-)-EXO EXO-2 3-CAMPHANEDIOL (+)-10-CAMPHORSULFONIMINE (-)-(8,8-DICHLOROCAMPHORYLSULFONYL)OXAZIRIDINE (1R)-(-)-10-Camphorsulfonic acid L(-)-10-Camphorsulfonyl chloride Rucaparib Camsylate D-CAMPHOR (1S)-(+)-Camphor-10-sulphonic acid (+)-(8,8-DICHLOROCAMPHORYLSULFONYL)OXAZIRIDINE (7,7-DIMETHYL-2-OXO-BICYCLO[2.2.1]HEPT-1-YL)-METHANESULFONYL CHLORIDE EUROPIUM D-3-TRIFLUOROACETYLCAMPHORATE EUROPIUM TRIS[3-(HEPTAFLUOROPROPYLHYDROXYMETHYLENE)-(+)-CAMPHORATE] L-10-CAMPHORSULFONIC ACID AMMONIUM SALT (1R)-(-)-CAMPHORQUINONE ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME,ISONITROSO-D-CAMPHOR ANTI-(1S)-(-)-CAMPHORQUINONE 3-OXIME 9&,ANTI-(1S)-(-)-CAMPHORQUINONE 3-OXIME, 99 % ANTI-(1S)-(-)-CAMPHORQUINONE 3-OXIME

  • (1R,E)-(+)-2,3-BORNANEDIONE 3-OXIME
  • (1R,E)-(+)-CAMPHORQUINONE 3-OXIME
  • ANTI-(1R)-(+)-2,3-BORNANEDIONE 3-OXIME
  • ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME
  • ISONITROSO-D-CAMPHOR
  • ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME, 99 %
  • (1R,E)-(+)-2,3-Bornanedione 3-oxime, anti-(1R
  • (1R,E)-(+)-2,3-Bornanedione 3-oxime, anti-(1R)-(+)-Camphorquinone 3-oxime
  • <i>anti</i>-(1<i>R</i>)-(+)-Camphorquinone 3-Oxime
  • (1R,4S,E)
  • -3-(Hydroxyimino)
  • (2Z)-2-hydroxyimino-4,7,7-trimethylbicyclo[2.2.1]heptan-3-one
  • Bicyclo[2.2.1]heptane-2,3-dione,1,7,7-trimethyl-, 3-oxime, (1R,3E,4S)-
  • anti-(1R)-(+)-Camphorquinone 3-Oxime &gt
  • (Z)-3-(hydroxyimino)-1,7,7-trimethylbicyclo[2.2.1]Heptan-2-one
  • 31571-14-9
  • Bicyclic Monoterpenes
  • Terpenes
  • Organic Building Blocks
  • Oximes
  • Asymmetric Synthesis
  • Chiral Building Blocks
  • Bicyclic Monoterpenes
  • Biochemistry
  • Terpenes