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104372-31-8((1R)-(-)-(10-Camphorsulfonyl)oxaziridine) Product Description

(1R)-(-)-(10-Camphorsulfonyl)oxaziridine Structure104372-31-8
CAS No.104372-31-8
Chemical Name:(1R)-(-)-(10-Camphorsulfonyl)oxaziridine
CBNumber:CB9768000
Molecular Formula:C10H15NO3S
Formula Weight:229.3
MOL File:Mol file
(1R)-(-)-(10-Camphorsulfonyl)oxaziridine Synonyms:
(-)-(2S,8AR)-(CAMPHORSULFONYL)OXAZIRIDINE
(2S,8AR)-(-)-(CAMPHORYLSULFONYL)OXAZIRIDINE
(1R)-(-)-(10-CAMPHORSULFONYL)OXAZIRIDINE
(1R)-(-)-(10-CAMPHORSULPHONYL)OXAZIRIDINE
(1R)-(-)-2,N-EPOXY-EXO-10,2-BORNANESULTAM
(1R)-(-)-(CAMPHORYLSULFONYL)OXAZIRIDINE
(R)-2,N-EPOXY-EXO-10,2-BORNANESULTAM
(-)-((CAMPHORYL) SULFONYL)OXAZIRIDINE

(1R)-(-)-(10-Camphorsulfonyl)oxaziridine Property

Melting point: 170-174 °C
Boiling point: 317.6±25.0 °C(Predicted)
alpha  -46.6 º (c=2, CHCl3 25 ºC)
Density  1.2486 (rough estimate)
refractive index  1.5060 (estimate)
Flash point: 170℃
storage temp.  2-8°C
solubility  Chloroform (Slightly), Methanol (Slightly)
pka -11.75±0.40(Predicted)
form  Powder
color  White
optical activity [α]20/D 44°, c = 2.2 in chloroform
BRN  6274369
CAS DataBase Reference 104372-31-8(CAS DataBase Reference)

Safety

Hazard Codes : Xi
Risk Statements : 36/37/38
Safety Statements : 26-36-24/25
WGK Germany : 3
F : 10
HS Code : 29349990

(1R)-(-)-(10-Camphorsulfonyl)oxaziridine Suppliers

Global( 242)Suppliers     
SupplierTelEmailCountryProdListAdvantage
Hubei wei shi reagent group ltd., company 027-027591017662853877621@qq.comChina 4819 58
Shanghai Zunlijia Life Technology Co., Ltd 021-34045219huji@zunlijia.comChina 10028 58
Hubei Nordina Biotechnology Co., Ltd.  n13164103386@163.comChina 2724 58
SHANGHAI KEAN TECHNOLOGY CO., LTD.  cooperation@kean-chem.comChina 40068 58
Bide Pharmatech Ltd. 400-164-7117product02@bidepharm.comChina 41463 60
Henan Anky Chemical Technology Co., Ltd.  3224305243@qq.comChina 2832 58
Accela ChemBio Inc. +1-858-6993322info@accelachem.comUnited States 19563 58
CHG Opto-Electronic Corporation Limited 25376531582537653158@qq.comChina 7605 58
104372-31-8((1R)-(-)-(10-Camphorsulfonyl)oxaziridine) Related Search:
(-)-(2S,8AR)-(CAMPHORSULFONYL)OXAZIRIDINE (2S,8AR)-(-)-(CAMPHORYLSULFONYL)OXAZIRIDINE (1R)-(-)-(10-CAMPHORSULFONYL)OXAZIRIDINE (1R)-(-)-(10-CAMPHORSULPHONYL)OXAZIRIDINE (1R)-(-)-2,N-EPOXY-EXO-10,2-BORNANESULTAM (1R)-(-)-(CAMPHORYLSULFONYL)OXAZIRIDINE (R)-2,N-EPOXY-EXO-10,2-BORNANESULTAM (-)-((CAMPHORYL) SULFONYL)OXAZIRIDINE (2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent] (-)-CAMPHORSULFONYLOXAZIRIDINE (-)-(2S,8aR)-(Camphorylsulfonyl)oxaziridine, 99+% ee, 99+% 4H-4a,7-Methanooxazirino3,2-i2,1benzisothiazole, tetrahydro-9,9-dimethyl-, 3,3-dioxide, (4aR,7S,8aR)- (2S,8AS)-(-)-(CAMPHORYLSULFONYL)OXAZIRIDINE (2S 8AR)-(-)-(CAMPHORYLSULFONYL)OXAZIRIDINE [ASYMMETRIC OXIDIZING GRADE] 98+% R-(10-Camphorsulfonyl)oxaziridine Tetrahydro-9,9-dimethyl-4H-4a,7-methanooxazirino[3,2-i][2,1]benzisothiazole 3,3-dioxide (10-camphorsulfonyl)oxaziridine (1R)-(-)-(Camphorylsulfonyl)oxaziridine, (1R)-(-)-2,N-Epoxy-exo-10,2-bornanesultam (-)-(2S,8AR)-(Camphorylsulfonyl)oxaziridine, 98%, ee:99+% (-)-(2S,8aR)-(Camphorylsulfonyl)oxaziridine, 99+% ee (-)-(2S,8aR)-(Camphorylsulfonyl)oxaziridine,98+% (4aR,7S,8aR)-Tetrahydro-9,9-diMethyl-4H-4a,7-Methano-1,2-oxazirino[3,2-i]-2,1-benzisothiazole 3,3-Dioxide (1R,2S)-(-)-2,N-Epoxy-10,2-caMphorsultaM, 96% (1R)-(-)-(10-Camphorsulfonyl)oxaziridine 1R)-(-)-(Camphorylsulfonyl)oxaziridine (R)-(10-Camphorsulfonyl)oxaziridine,99%e.e. 7,7-dimethyl-4-(2-oxaziridinylsulfonylmethyl)-3-bicyclo[2.2.1]heptanone (1R)-(-)-(10-Camphorsulfonyl)oxaziridin (2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent]> (-)-(2S,8aR)-(Camphorylsulfonyl)oxaziridine 4H-4a,7-Methanooxazirino[3,2-i][2,1]benzisothiazole, tetrahydro-9,9-dimethyl-, 3,3-dioxide, (4aR,7S,8aR)- (9CI, ACI) Tetrahydro-9,9-dimethyl-4H-4a,7-methanooxazirino3,2-i2,1benzisothiazole 3,3-dioxide (4aR,7S,8aR)- 104372-31-8 Oxidation Bicyclic Monoterpenes Terpenes Sulfur Compounds (for Synthesis) Asymmetric Synthesis Chiral Catalysts, Ligands, and Reagents Hydroxylation Biochemistry Oxidation Sulfur Compounds (for Synthesis) Synthetic Organic Chemistry Terpenes Intermediates & Fine Chemicals Pharmaceuticals Asymmetric Synthesis Bicyclic Monoterpenes chiral Chiral Reagents
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