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(+)-10,2-Camphorsultam
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(+)-10,2-Camphorsultam

CAS: 108448-77-7

Ref. 3D-FC59960

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Estimated delivery in United States, on Thursday 9 Jan 2025

Product Information

Name:
(+)-10,2-Camphorsultam
Synonyms:
  • (2S)-Bornane-10,2-sultam(1R,5S)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]decane 3,3-Dioxide
  • [3aR-(3aalpha,6alpha,7abeta)]-Hexahydro-8,8-dimethyl-3H-3a,6-methano-2,1-benzisothiazole 2,2-dioxide
  • (1R)-(+)-2,10-Camphorsultam
  • (1R)-(+)-2,10,Camphor sultam
  • 8,8-Dimethylhexahydro-3A,6-Methano-2,1-Benzothiazole 2,2-Dioxide
  • (3aR,6S,7aS)-8,8-dimethylhexahydro-3a,6-methano-2,1-benzothiazole 2,2-dioxide
  • (3aR,6R,7aR)-8,8-dimethylhexahydro-3a,6-methano-2,1-benzisothiazole 2,2-dioxide
  • (+)-Camphorsultam
Description:

(+)-10,2-Camphorsultam is an isoxazolidine of the l-glutamic acid type. It has a chiral carbon atom and, in addition to the usual carboxyl group, has an amino group. The enantiomers of (+)-10,2-camphorsultam are made in a stereoselective manner by using potassium carbonate as a catalyst. This compound can be used for synthesis reactions such as aminations, enantiomer separations, and cycloadditions. In addition to this it functions as a chiral auxiliary in 1,3-dipolar cycloadditions with carbonyl derivatives.

Notice:
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Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
215.31 g/mol
Formula:
C10H17NO2S
Purity:
Min. 95%
MDL:
Melting point:
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Flash point:
Density:
Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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