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(1R)-(-)-(10-Camphorsulfonyl)oxaziridine_Molecular_structure_CAS_104372-31-8)
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(1R)-(-)-(10-Camphorsulfonyl)oxaziridine

Catalog No. 349003 Name Sigma Aldrich
CAS Number 104372-31-8 Website http://www.sigmaaldrich.com
M. F. C10H15NO3S Telephone 1-800-521-8956
M. W. 229.296 Fax
Purity Email
Storage Chembase ID: 146704

SYNONYMS

Title
(1R)-(-)-(10-樟脑磺)哑嗪
IUPAC name
(1R,8R)-11,11-dimethyl-5-oxa-3λ6-thia-4-azatetracyclo[6.2.1.01,6.04,6]undecane-3,3-dione
IUPAC Traditional name
(1R,8R)-11,11-dimethyl-5-oxa-3λ6-thia-4-azatetracyclo[6.2.1.01,6.04,6]undecane-3,3-dione
Synonyms
(1R)-(-)-2,N-Epoxy-exo-10,2-bornanesultam
(1R)-(-)-2,N-环氧基-exo-10,2-莰烷磺内酰胺
(1R)-(-)-(Camphorylsulfonyl)oxaziridine
(1R)-(-)-樟脑磺哑嗪

DATABASE IDS

Beilstein Number 6274369
PubChem SID 24861490
CAS Number 104372-31-8
MDL Number MFCD00075428

PROPERTIES

Empirical Formula (Hill Notation) C10H15NO3S
Optical Rotation [α]20/D -44°, c = 2.2 in chloroform
MSDS Link Download
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Packaging
1 g in glass bottle
250 mg in glass bottle
Application
Reactant involved in:
• Asymmetric synthesis of proton pump inhibitors1
• Asymmetric synthesis of polyhydroxylated pyrrolidines2
• Diastereoselective hydroxylation of chlorophylls a and b enolate anions3Used in impregnated silica nanoparticles for removal of sulfur mustard from wastewater4Used to modify blebbistatin for investigations of myosin inhibitor design5
Description (简体中文)
包装
1 g in glass bottle
250 mg in glass bottle
Application
Reactant involved in:
• Asymmetric synthesis of proton pump inhibitors1
• Asymmetric synthesis of polyhydroxylated pyrrolidines2
• Diastereoselective hydroxylation of chlorophylls a and b enolate anions3Used in impregnated silica nanoparticles for removal of sulfur mustard from wastewater4Used to modify blebbistatin for investigations of myosin inhibitor design5

REFERENCES