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

CAS No.: 104372-31-8

Chemical Name:: (1R)-(-)-(10-Camphorsulfonyl)oxaziridine

Synonyms: (-)-CAMPHORSULFONYLOXAZIRIDINE;(10-camphorsulfonyl)oxaziridine;R-(10-Camphorsulfonyl)oxaziridine;(R)-2,N-EPOXY-EXO-10,2-BORNANESULTAM;(-)-((CAMPHORYL) SULFONYL)OXAZIRIDINE;(1R)-(-)-(CAMPHORYLSULFONYL)OXAZIRIDINE;(1R)-(-)-(10-Camphorsulfonyl)oxaziridin;(1R)-(-)-(10-CAMPHORSULFONYL)OXAZIRIDINE;(1R)-(-)-2,N-EPOXY-EXO-10,2-BORNANESULTAM;(1R)-(-)-(10-CAMPHORSULPHONYL)OXAZIRIDINE

CBNumber:: CB9768000

Molecular Formula:: C10H15NO3S

Molecular Weight:: 229.3

MOL File:: 104372-31-8.mol

Modify Date:: 2023/8/17 18:11:45

Request For Quotation

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

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

Risk and Safety Statements

Symbol(GHS)

GHS07

Signal word

Warning

Hazard statements

H302-H315-H319-H335

Precautionary statements

P261-P280-P301+P312-P302+P352-P305+P351+P338

Hazard Codes

Risk Statements

36/37/38

Safety Statements

26-36-24/25

WGK Germany

HS Code

29349990

NFPA 704

	1
0		0

(1R)-(-)-(10-Camphorsulfonyl)oxaziridine price More Price(4)

Manufacturer	Product number	Product description	CAS number	Packaging	Price	Updated	Buy
Sigma-Aldrich	349003	(1R)-(−)-(10-Camphorsulfonyl)oxaziridine	104372-31-8	1G	₹8350	2022-06-14	Buy
Sigma-Aldrich(India)	349003	(1R)-(−)-(10-Camphorsulfonyl)oxaziridine	104372-31-8	1G	₹8350	2022-06-14	Buy
TCI Chemicals (India)	C1327	(2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent]	104372-31-8	1G	₹6200	2022-05-26	Buy
TCI Chemicals (India)	C1327	(2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent]	104372-31-8	5G	₹14500	2022-05-26	Buy

Product number	Packaging	Price	Buy
349003	1G	₹8350	Buy
349003	1G	₹8350	Buy
C1327	1G	₹6200	Buy
C1327	5G	₹14500	Buy

(1R)-(-)-(10-Camphorsulfonyl)oxaziridine Chemical Properties,Uses,Production

Chemical Properties

White crystalline powder

Uses

(1R)-(-)-(10-Camphorsulfonyl)oxaziridine is a useful synthetic intermediate. Used for asymmetric hydroxylation.

(1R)-(-)-(10-Camphorsulfonyl)oxaziridine Preparation Products And Raw materials

Raw materials

(+)-10-CAMPHORSULFONIMINE

Preparation Products

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

Global( 239)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
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
Pharmaffiliates Analytics and Synthetics P. Ltd	+91-172-5066494	Haryana, India	6773	58	Inquiry
Changzhou Chontech Baocheng Chemical Co.,Ltd	+86-51982698291; +undefined15295095616	China	73	58	Inquiry
Hebei Mojin Biotechnology Co., Ltd	+86 13288715578 +8613288715578	China	12447	58	Inquiry

Supplier	Advantage
CHEMSWORTH	30
A.J Chemicals	58
CLEARSYNTH LABS LTD.	58
TCI Chemicals (India) Pvt. Ltd.	58
Reax Chemicals	58
Pharma Affiliates	58
Souvenier Chemicals	58
Pharmaffiliates Analytics and Synthetics P. Ltd	58
Changzhou Chontech Baocheng Chemical Co.,Ltd	58
Hebei Mojin Biotechnology Co., Ltd	58

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

(1R)-(-)-(10-Camphorsulfonyl)oxaziridine(104372-31-8)MS (1R)-(-)-(10-Camphorsulfonyl)oxaziridine(104372-31-8)¹HNMR (1R)-(-)-(10-Camphorsulfonyl)oxaziridine(104372-31-8)IR1 (1R)-(-)-(10-Camphorsulfonyl)oxaziridine(104372-31-8)IR2

104372-31-8((1R)-(-)-(10-Camphorsulfonyl)oxaziridine)Related Search:

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(1S)-(+)-(10-CAMPHORSULFONYL)OXAZIRIDINE,(1S)-(+)-(10-Camphorsulfonyl)oxaziridine (1S)-(+)-2,N-Epoxy-exo-10,2-bornanesultam Camphor DL-Camphor EPOXY 1-PENTANESULFONAMIDE

4-04-00-00045 (Beilstein Handbook Reference) 1-HEXANESULFONAMIDE PROPANE-1-SULFONAMIDE

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(-)-(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