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

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

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

MDL Number:: MFCD00075428

MOL File:: 104372-31-8.mol

Last updated:2023-08-17 18:11:45

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(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(34)

Manufacturer	Product number	Product description	CAS number	Packaging	Price	Updated	Buy
Sigma-Aldrich	349003	(1R)-(?)-(10-Camphorsulfonyl)oxaziridine	104372-31-8	1g	$109.2	2024-03-01	Buy
TCI Chemical	C1327	(2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent] >95.0%(T)	104372-31-8	1g	$30	2024-03-01	Buy
TCI Chemical	C1327	(2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent] >95.0%(T)	104372-31-8	5g	$88	2024-03-01	Buy
Alfa Aesar	H59544	(1R,2S)-(-)-2,N-Epoxy-10,2-camphorsultam, 96%	104372-31-8	1g	$93.65	2024-03-01	Buy
TRC	C175095	(1R)-(-)-(10-Camphorsulfonyl)oxaziridine	104372-31-8	50g	$405	2021-12-16	Buy

Product number	Packaging	Price	Buy
349003	1g	$109.2	Buy
C1327	1g	$30	Buy
C1327	5g	$88	Buy
H59544	1g	$93.65	Buy
C175095	50g	$405	Buy

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

Chemical Properties

White crystalline powder

Uses

Reactant involved in:

Asymmetric synthesis of proton pump inhibitors
Asymmetric synthesis of polyhydroxylated pyrrolidines
Diastereoselective hydroxylation of chlorophylls a and b enolate anions

Used in impregnated silica nanoparticles for removal of sulfur mustard from wastewater

Used to modify blebbistatin for investigations of myosin inhibitor design

Uses

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

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

Synthesis of (1R)-(-)-(10-Camphorsulfonyl)oxaziridine from (+)-10-CAMPHORSULFONIMINE

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

Raw materials

(+)-10-CAMPHORSULFONIMINE

Preparation Products

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

Global( 240)Suppliers

Supplier	Tel	Email	Country	ProdList	Advantage
Changzhou Chontech Baocheng Chemical Co.,Ltd	+86-51982698291; +undefined15295095616	info@hhbhswkj.com	China	73	58
Hebei Mojin Biotechnology Co., Ltd	+8613288715578	sales@hbmojin.com	China	12453	58
Capot Chemical Co.,Ltd.	571-85586718 +8613336195806	sales@capotchem.com	China	29797	60
Shanghai Daken Advanced Materials Co.,Ltd	+86-371-66670886	info@dakenam.com	China	15371	58
Nanjing ChemLin Chemical Industry Co., Ltd.	025-83697070	product@chemlin.com.cn	CHINA	3012	60
ATK CHEMICAL COMPANY LIMITED	+undefined-21-51877795	ivan@atkchemical.com	China	32480	60
career henan chemical co	+86-0371-86658258	sales@coreychem.com	China	29914	58
Accela ChemBio Inc.	(+1)-858-699-3322	info@accelachem.com	United States	19965	58
Hebei Guanlang Biotechnology Co., Ltd.	+86-19930503282	alice@crovellbio.com	China	8822	58
Xi'an Kono chem co., Ltd.,	029-86107037 13289246953	info@konochemical.com	China	2995	58

Supplier	Advantage
Changzhou Chontech Baocheng Chemical Co.,Ltd	58
Hebei Mojin Biotechnology Co., Ltd	58
Capot Chemical Co.,Ltd.	60
Shanghai Daken Advanced Materials Co.,Ltd	58
Nanjing ChemLin Chemical Industry Co., Ltd.	60
ATK CHEMICAL COMPANY LIMITED	60
career henan chemical co	58
Accela ChemBio Inc.	58
Hebei Guanlang Biotechnology Co., Ltd.	58
Xi'an Kono chem co., Ltd.,	58

View Lastest Price from (1R)-(-)-(10-Camphorsulfonyl)oxaziridine manufacturers

Update time	Product	Price	Min. Order	Purity	Supply Ability	Manufacturer
2023-08-18	(1R)-(-)-(10-Camphorsulfonyl)oxaziridine 104372-31-8	US $0.00 / KG	1KG	99%	50000KG/month	Hebei Mojin Biotechnology Co., Ltd
2023-02-18	(1R)-(-)-(10-Camphorsulfonyl)oxaziridine 104372-31-8	US $0.00-0.00 / kg	1kg	98%	kgs	Aromsyn Co., Ltd.
2022-09-19	(1(R))-()-(10-Camphorsulfonyl)oxaziridine 104372-31-8	US $20.00 / kg	1kg	99%	5000 tons	Hebei Duling International Trade Co. LTD

(1R)-(-)-(10-Camphorsulfonyl)oxaziridine
104372-31-8
US $0.00 / KG
99%
Hebei Mojin Biotechnology Co., Ltd

(1R)-(-)-(10-Camphorsulfonyl)oxaziridine
104372-31-8
US $0.00-0.00 / kg
98%
Aromsyn Co., Ltd.

(1(R))-()-(10-Camphorsulfonyl)oxaziridine
104372-31-8
US $20.00 / kg
99%
Hebei Duling International Trade Co. LTD

(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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Cyclopentylamine Ethanesulfonamide 3-METHYLCYCLOHEXYLAMINE BORNYLAMINE 2-Ethyl-1-hexanethiol

(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