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

(1S)-(+)-(Camphorylsulfonyl)oxaziridine Struktur
104322-63-6
CAS-Nr.
104322-63-6
Englisch Name:
(1S)-(+)-(Camphorylsulfonyl)oxaziridine
Synonyma:
(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
Summenformel:
C10H15NO3S
Molgewicht:
229.3
MOL-Datei:
104322-63-6.mol

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

Schmelzpunkt:
172-174 °C(lit.)
alpha 
45 º (c=2, chloroform)
Siedepunkt:
317.6±25.0 °C(Predicted)
Dichte
1.2486 (rough estimate)
Brechungsindex
1.5060 (estimate)
storage temp. 
2-8°C
L?slichkeit
Chloroform (Sparingly), Methanol (Slightly)
pka
-11.75±0.40(Predicted)
Aggregatzustand
Crystals or Crystalline Powder
Farbe
White
Optische Aktivit?t
[α]28/D +45°, c = 2 in chloroform
BRN 
6274370
CAS Datenbank
104322-63-6(CAS DataBase Reference)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
S-S?tze: 22-24/25
WGK Germany  3
10
HS Code  29309090
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizit?t (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" />
Sicherheit
P261 Einatmen von Staub vermeiden.
P271 Nur im Freien oder in gut belüfteten R?umen verwenden.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

(1S)-(+)-(Camphorylsulfonyl)oxaziridine Chemische Eigenschaften,Einsatz,Produktion Methoden

S-S?tze Betriebsanweisung:

S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.

Chemische Eigenschaften

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

Verwenden

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

Synthese

The enantiopure (1S)-(+)-(Camphorylsulfonyl)oxaziridine and (1R)-(-)-(10-Camphorsulfonyl)oxaziridine and [(8,8- dichlorocamphor)sulfonyl]oxaziridines (2) are commercially available. They can also be prepared on a large scale via the oxidation of corresponding camphorsulfonimines with buffered Potassium Monoperoxysulfate (Oxone) or buffered peracetic acid. Since oxidation takes place from the endo face of the C=N double bond, only a single oxaziridine isomer is obtained. The precursor camphorsulfonimines can be prepared in 3 steps (>80% yield) from inexpensive (+)- and (-)-10-Camphorsulfonic Acids. A variety of (camphorylsulfonyl)oxaziridine derivatives such as (2)-(4) are also readily available via the functionalization of the camphorsulfonimines followed by oxidation.
(1S)-( )-(Camphorylsulfonyl)oxaziridine

Einzelnachweise

1. Mergelsberg, I.; Gala, D.; Scherer, D.; DiBenedetto, D.; Tanner TL 1992, 33, 161.
2. Davis, F. A.; Kumar, A.; Chen, B.-C. JOC 1991, 56, 1143.
3. Chen, B.-C.; Weismiller, M. C.; Davis, F. A.; Boschelli, D.; Empfield, J. R.; Smith, III, A. B. T 1991, 47, 173.

(1S)-(+)-(Camphorylsulfonyl)oxaziridine Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


(1S)-(+)-(Camphorylsulfonyl)oxaziridine Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 268)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Changzhou Chontech Baocheng Chemical Co.,Ltd
+86-51982698291; +undefined15295095616
info@hhbhswkj.com China 73 58
Zibo Hangyu Biotechnology Development Co., Ltd
+86-0533-2185556 +8617865335152
Mandy@hangyubiotech.com China 10986 58
Hebei Jingbo New Material Technology Co., Ltd
+8619931165850
hbjbtech@163.com China 1000 58
Hebei Saisier Technology Co., LTD
+86-18400010335 +86-18034520335
admin@hbsaisier.cn China 1015 58
HebeiShuoshengImportandExportco.,Ltd
+86-18532138899 +86-18532138899
L18532138899@163.com China 939 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806
sales@capot.com China 29793 60
Shanghai Daken Advanced Materials Co.,Ltd
+86-371-66670886
info@dakenam.com China 18945 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21634 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795
ivan@atkchemical.com China 32956 60
career henan chemical co
+86-0371-86658258 +8613203830695
sales@coreychem.com China 29879 58

104322-63-6()Verwandte Suche:


  • (+)-(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
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