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

(1S)-(+)-(Camphorylsulfonyl)oxaziridine Structure
CAS No.
104322-63-6
Chemical Name:
(1S)-(+)-(Camphorylsulfonyl)oxaziridine
Synonyms
(S)-(+)-(Camphorsulfonyl)Oxazi;(+)-(Camphorsulfonyl)oxaziridine;S-(10-Camphorsulfonyl)oxaziridine;(S)-(+)-(CAMPHORSULFONYL)OXAZIRIDINE;(S)-2,N-EPOXY-EXO-10,2-BORNANESULTAM;(+)-((CAMPHORYL)SULFONYL)OXAZIRIDINE;(S)-(+)-(Camphorylsulfonyl)oxaziridine;(1S)-(+)-(CAMPHORYLSULFONYL)OXAZIRIDINE;(1S)-(+)-(10-CAMPHORSULFONYL) OXAZIRINE;(1S)-(+)-(1-Camphorsulfonyl)oxaziridine
CBNumber:
CB3447891
Molecular Formula:
C10H15NO3S
Molecular Weight:
229.3
MOL File:
104322-63-6.mol
Modify Date:
2024/8/30 21:22:42

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

Melting point 172-174 °C(lit.)
alpha 45 º (c=2, chloroform)
Boiling point 317.6±25.0 °C(Predicted)
Density 1.2486 (rough estimate)
refractive index 1.5060 (estimate)
storage temp. 2-8°C
solubility Chloroform (Sparingly), Methanol (Slightly)
pka -11.75±0.40(Predicted)
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

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P271-P280
Safety Statements  22-24/25
WGK Germany  3
10
HS Code  29309090
NFPA 704
0
1 0

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

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 345350 (1S)-(+)-(10-Camphorsulfonyl)oxaziridine 104322-63-6 1G ₹13671.98 2022-06-14 Buy
TCI Chemicals (India) C1326 (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent] 104322-63-6 1G ₹3900 2022-05-26 Buy
TCI Chemicals (India) C1326 (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent] 104322-63-6 5G ₹8800 2022-05-26 Buy
Product number Packaging Price Buy
345350 1G ₹13671.98 Buy
C1326 1G ₹3900 Buy
C1326 5G ₹8800 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

Global( 262)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CHEMSWORTH +91-261-2397244 New Delhi, India 6707 30 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
Reax Chemicals 08048372701Ext 416 Hyderabad, India 4223 58 Inquiry
Pharma Affiliates 172-5066494 Haryana, India 6761 58 Inquiry
Souvenier Chemicals 08048372762Ext 645 Mumbai, India 396 58 Inquiry
Changzhou Chontech Baocheng Chemical Co.,Ltd +86-51982698291; +undefined15295095616 China 73 58 Inquiry
Zibo Hangyu Biotechnology Development Co., Ltd +86-0533-2185556 +8617865335152 China 10991 58 Inquiry
(+)-(2R,8AS)-(CAMPHORYLSULFONYL)OXAZIRIDINE (2R,8AS)-(+)-(CAMPHORYLSULFONYL)OXAZIRIDINE (1S)-(+)-2,N-EPOXY-EXO-10,2-BORNANESULTAM (IS)-(+)-(10-Camphorsulfonyl)oxaziridine S-(10-Camphorsulfonyl)oxaziridine (4aS,7R,8aS)-9,9-DiMethyltetrahydro-4H-4a,7-Methanobenzo[c][1,2]oxazireno[2,3-b]isothiazole 3,3-dioxide (+)-(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 (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+% (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)-(+)-(CAMPHORYLSULFONYL)OXAZIRIDINE (1S)-(+)-(10-CAMPHORSULFONYL)OXAZIRIDINE (1S)-(+)-(10-CAMPHORSULPHONYL)OXAZIRIDINE (S)-(+)-(CAMPHORSULFONYL)OXAZIRIDINE (S)-2,N-EPOXY-EXO-10,2-BORNANESULTAM (+)-((CAMPHORYL)SULFONYL)OXAZIRIDINE (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] (S)-(10-Camphorsulfonyl)oxaziridine,99%e.e. (+)-(2R, 8aS)-(Camphorylsulfonyl)oxaziridine, 99+%, (99+% e.e.) (1S)-(+)-(1-Camphorsulfonyl)oxaziridine (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine[AsymmetricOxidizingReagent]> 4H-4a,7-Methanooxazirino[3,2-i][2,1]benzisothiazole, tetrahydro-9,9-dimethyl-, 3,3-dioxide, (4aS,7R,8aS)- CAS104322-63-6 (1S)-(+)-(Camphorylsulfonyl)oxaziridine (+)-(2R,8aS)-(Camphorylsulfonyl)oxaziridine (+)-(Camphorsulfonyl)oxaziridine (4aS,7S,8aS)-9,9-dimethyltetrahydro-4H-4a,7-methanobenzo[c][1,2]oxazireno[2,3-b]isothiazole 3,3-dioxide (1S,8R)-11,11-dimethyl-5-oxa-3λ?-thia-4-azatetracyclo[6.2.1.0?,?.0?,?]undecane-3,3-dione (1S,8R)-11,11-dimethyl-5-oxa-3λ?-thia-4-azatetracyclo[6.2.1.01,?.0?,?]undecane-3,3-dione 104322-63-6 C10H15NO3S Hydroxylation Asymmetric Synthesis Sulfur Compounds (for Synthesis) Bicyclic Monoterpenes Oxidation Terpenes Chiral Catalysts, Ligands, and Reagents Intermediates & Fine Chemicals Pharmaceuticals Chiral Reagents pharmacetical chiral Asymmetric Synthesis Bicyclic Monoterpenes