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(1S)-(+)-(Camphorylsulfonyl)oxaziridine

(1S)-(+)-(Camphorylsulfonyl)oxaziridine
(1S)-(+)-(Camphorylsulfonyl)oxaziridine structure
CAS No.
104322-63-6
Chemical Name:
(1S)-(+)-(Camphorylsulfonyl)oxaziridine
Synonyms
(S)-(+)-(Camphorsulfonyl)Oxazi;S-(10-Camphorsulfonyl)oxaziridine;(+)-((CAMPHORYL)SULFONYL)OXAZIRIDINE;(S)-(+)-(CAMPHORSULFONYL)OXAZIRIDINE;(S)-2,N-EPOXY-EXO-10,2-BORNANESULTAM;(S)-(+)-(Camphorylsulfonyl)oxaziridine;(1S)-(+)-(CAMPHORYLSULFONYL)OXAZIRIDINE;(1S)-(+)-(10-CAMPHORSULFONYL) OXAZIRINE;(1S)-(+)-(1-Camphorsulfonyl)oxaziridine;(IS)-(+)-(10-Camphorsulfonyl)oxaziridine
CBNumber:
CB3447891
Molecular Formula:
C10H15NO3S
Formula Weight:
229.3
MOL File:
104322-63-6.mol

(1S)-(+)-(Camphorylsulfonyl)oxaziridine Properties

Melting point:
172-174 °C(lit.)
alpha 
45 º (c=2, chloroform)
Density 
1.2486 (rough estimate)
refractive index 
1.5060 (estimate)
storage temp. 
2-8°C
form 
Crystals or Crystalline Powder
color 
White
optical activity
[α]28/D +45°, c = 2 in chloroform
BRN 
6274370
CAS DataBase Reference
104322-63-6(CAS DataBase Reference)

SAFETY

Safety Statements  22-24/25
WGK Germany  3
10
HS Code  29309090

(1S)-(+)-(Camphorylsulfonyl)oxaziridine price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 345350 (1S)-(+)-(10-Camphorsulfonyl)oxaziridine 104322-63-6 1g $177 2018-11-13 Buy
TCI Chemical C1326 (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent] >95.0%(T) 104322-63-6 1g $43 2018-11-22 Buy
TCI Chemical C1326 (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent] >95.0%(T) 104322-63-6 5g $139 2018-11-22 Buy

(1S)-(+)-(Camphorylsulfonyl)oxaziridine Chemical Properties,Uses,Production

Chemical Properties

(1S)-(+)-(Camphorylsulfonyl)oxaziridine is white crystall powder

Uses

(1S)-(+)-(Camphorylsulfonyl)oxaziridine is a useful synthetic intermediate. Used for asymmetric hydroxylation

(1S)-(+)-(Camphorylsulfonyl)oxaziridine Preparation Products And Raw materials

Raw materials

Preparation Products


(1S)-(+)-(Camphorylsulfonyl)oxaziridine Suppliers

Global( 151)Suppliers
Supplier Tel Fax Email Country ProdList Advantage
Henan DaKen Chemical CO.,LTD.
+86-371-55531817
info@dakenchem.com CHINA 21930 58
Henan Tianfu Chemical Co.,Ltd.
0371-55170693
0371-55170693 info@tianfuchem.com CHINA 20680 55
Mainchem Co., Ltd.
+86-0592-6210733
+86-0592-6210733 sales@mainchem.com CHINA 32457 55
ATK CHEMICAL COMPANY LIMITED
+86 21 5161 9050/ 5187 7795
+86 21 5161 9052/ 5187 7796 ivan@atkchemical.com CHINA 24196 60
career henan chemical co
+86-371-86658258
sales@coreychem.com CHINA 20516 58
Kono Chem Co., Ltd
+86-132 8924 6953
info@konochemical.com CHINA 2144 58
Chemwill Asia Co.,Ltd.
86-21-51086038
86-21-51861608 chemwill_asia@126.com;sales@chemwill.com;chemwill@hotmail.com;chemwill@gmail.com CHINA 23982 58
Accela ChemBio Inc.
(+1)-858-699-3322
(+1)-858-876-1948 info@accelachem.com United States 12233 58
PingHeAnKang Pharmaceutical Co., Ltd. 17308063174 ; 18086832706
028-89642128 phakzjtxs@phak.cn China 138 58
J & K SCIENTIFIC LTD. 400-666-7788 +86-10-82848833
+86-10-82849933 jkinfo@jkchemical.com;market6@jkchemical.com China 96815 76

View Lastest Price from (1S)-(+)-(Camphorylsulfonyl)oxaziridine manufacturers

Image Release date Product Price Min. Order Purity Supply Ability Manufacturer
2018-08-07 (1S)-(+)-(Camphorylsulfonyl)oxaziridine
104322-63-6
US $1.00 / KG 1KG 98% 20KG career henan chemical co

(1S)-(+)-(Camphorylsulfonyl)oxaziridine Spectrum


104322-63-6((1S)-(+)-(Camphorylsulfonyl)oxaziridine)Related Search:


  • (1S)-(+)-(Camphorylsulfonyl)oxaziridine, (1S)-(+)-2,N-Epoxy-exo-10,2-bornanesultam
  • (1α,5β,7α)-10,10-Dimethyl-4,5-epoxy-3-thia-4-azatricyclo[5.2.1.01,5]decane3,3-dioxide
  • (3aS)-9,9-Dimethyloctahydro-3aβ,6β-methano-1,7aα-epoxy-2,1-benzisothiazole 2,2-dioxide
  • (4aS,7R,8aS)-5,6,7,8-Tetrahydro-9,9-dimethyl-4H-4a,7-methanooxazirino[3,2-i][2,1]benzoisothiazole 3,3-dioxide
  • (4aS,7R,8aS)-9,9-Dimethyl-4H-4a,7-methanotetrahydrooxazirino[3,2-i][2,1]benzisothiazole 3,3-dioxide
  • (8aS)-5,6,7,8-Tetrahydro-9,9-dimethyl-4H-4aβ,7β-methanooxazirino[3,2-i][2,1]benzisothiazole 3,3-dioxide
  • (+)-(2R,8aS)-(Camphorylsulfonyl)oxaziridine,98+%
  • (IS)-(+)-(10-Camphorsulfonyl)oxaziridine
  • S-(10-Camphorsulfonyl)oxaziridine
  • (1S)-(+)-(CAMPHORYLSULFONYL)OXAZIRIDINE
  • (1S)-(+)-(10-CAMPHORSULFONYL)OXAZIRIDINE
  • (+)-(2R,8AS)-(CAMPHORYLSULFONYL)OXAZIRIDINE
  • (2R,8AS)-(+)-(CAMPHORYLSULFONYL)OXAZIRIDINE
  • (1S)-(+)-2,N-EPOXY-EXO-10,2-BORNANESULTAM
  • (+)-(2R,8aS)-10-(CaMphorylsulfonyl)oxaziridine
  • (4aS,7R,8aS)-Tetrahydro-9,9-diMethyl-4H-4a,7-Methanooxazirino[3,2-i][2,1]benzisothiazole 3,3-Dioxide
  • (4aS,7R,8aS)-9,9-DiMethyltetrahydro-4H-4a,7-Methanobenzo[c][1,2]oxazireno[2,3-b]isothiazole 3,3-dioxide
  • (4AS,7R,8aS)-9,9-Dimethyltetrahydro-4H-4a,7-methanobenzo-[c][1,2]oxazireno[2,3-b]isothiazole 3,3-
  • (1S)-(+)-(10-Camphorsulfonyl)oxaziridine (1S)-(+)-(Camphorylsulfonyl)oxaziridine
  • (S)-(+)-(Camphorylsulfonyl)oxaziridine
  • (4AS,7R,8aS)-9,9-Dimethyltetrahydro-4H-4a,7-methanobenzo-[c][1,2]oxazireno[2,3-b]isothiazole 3
  • (1S)-(+)-(10-CAMPHORSULPHONYL)OXAZIRIDINE
  • (+)-((CAMPHORYL)SULFONYL)OXAZIRIDINE
  • (S)-(+)-(CAMPHORSULFONYL)OXAZIRIDINE
  • (S)-2,N-EPOXY-EXO-10,2-BORNANESULTAM
  • (1S)-(+)-(10-Camphorsulfonyl)oxaziridine (1S)-(+)-2,N-Epoxy-exo-10,2-bornanesultam
  • (+)-(2R,8aS)-(Camphorylsulfonyl)oxaziridine, 99+% ee, 99+%
  • (S)-(+)-(Camphorsulfonyl)Oxazi
  • (1S)-(+)-(10-CAMPHORSULFONYL) OXAZIRINE
  • (2R 8AS)-(+)-(CAMPHORYLSULFONYL)OXAZIRIDINE [ASYMMETRIC OXIDIZING GR]
  • (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent]
  • 104322-63-6
  • C10H15NO3S
  • Chiral Catalysts, Ligands, and Reagents
  • Hydroxylation
  • Asymmetric Synthesis
  • Sulfur Compounds (for Synthesis)
  • Bicyclic Monoterpenes
  • Oxidation
  • Terpenes
  • (S)-(10-Camphorsulfonyl)oxaziridine,99%e.e.
  • (+)-(2R, 8aS)-(Camphorylsulfonyl)oxaziridine, 99+%, (99+% e.e.)
  • (1S)-(+)-(1-Camphorsulfonyl)oxaziridine
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • pharmacetical
  • chiral
  • Chiral Reagents
  • Asymmetric Synthesis
  • Bicyclic Monoterpenes
  • Biochemistry
  • Oxidation
  • Sulfur Compounds (for Synthesis)
  • Synthetic Organic Chemistry
  • Terpenes
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