(1S)-(-)-CAMPHORSULFONYLIMINE

Product Name: (1S)-(-)-CAMPHORSULFONYLIMINE
CAS No.: 60886-80-8
Chemical Name: (1S)-(-)-CAMPHORSULFONYLIMINE
Synonyms: 97.0%(N);Bornanesultam;SCamphorsulfonylimine;(-)-10-CAMPHORSULFONIMINE;(-)-10-Camphorsulfonimine;D-(-)-CAMPHORSULFONYL IMINE;(-)-10-Camphorsulfonylimine;(1S)-(-)-CAMPHORSULFONYLIMINE;(IS)-(-)-Camphorsulfonylimine;(-)-10-Camphorsulfonimine >
CBNumber: CB8404363
Molecular Formula: C10H15NO2S
Formula Weight: 213.3
MOL File: 60886-80-8.mol

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(1S)-(-)-CAMPHORSULFONYLIMINE Property

Melting point:: 228-230 °C (lit.)
Boiling point:: 337℃
Density: 1.50
refractive index: -31 ° (C=2, CHCl3)
Flash point:: 158℃
storage temp.: Sealed in dry,Room Temperature
solubility: Acetone, Dichloromethane, Hot Methanol
form: Solid
pka: -1.63±0.40(Predicted)
color: White Cyrstalline
optical activity: [α]19/D 34°, c = 1 in chloroform
BRN: 85296
CAS DataBase Reference: 60886-80-8(CAS DataBase Reference)

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Safety

Hazard Codes: Xi
Risk Statements: 36/37/38
Safety Statements: 26-36
WGK Germany: 3
HS Code: 2934.99.9001

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 318361
Product name: (1S)-(?)-Camphorsulfonylimine
Purity: 99%
Packaging: 1g
Price: $18.32
Updated: 2024/03/01

TCI Chemical

Product number: C1393
Product name: (-)-10-Camphorsulfonimine
Purity: >98.0%(HPLC)(N)
Packaging: 5g
Price: $123
Updated: 2024/03/01

Alfa Aesar

Product number: B20823
Product name: (1S)-(-)-Camphorsulfonylimine, 98+%
Packaging: 1g
Price: $38.65
Updated: 2024/03/01

Alfa Aesar

Product number: B20823
Product name: (1S)-(-)-Camphorsulfonylimine, 98+%
Packaging: 5g
Price: $126.65
Updated: 2024/03/01

Alfa Aesar

Product number: B20823
Product name: (1S)-(-)-Camphorsulfonylimine, 98+%
Packaging: 25g
Price: $568.65
Updated: 2024/03/01

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(1S)-(-)-CAMPHORSULFONYLIMINE Chemical Properties,Usage,Production

Chemical Properties

White Cyrstalline Solid

Uses

A useful synthetic intermediate. Used for asymmetric hydroxylation.

Uses

(1S)-(-)-Camphorsulfonylimine is a useful synthetic intermediate. Used for asymmetric hydroxylation

(1S)-(-)-CAMPHORSULFONYLIMINE Preparation Products And Raw materials

Raw materials

Preparation Products

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(1S)-(-)-CAMPHORSULFONYLIMINE Suppliers

Americas 1 Belgium 1 Canada 2 China 67 Europe 2 France 2 Germany 6 India 6 Japan 1 Switzerland 1 The Netherlands 2 United Kingdom 7 United States 21 Global 119

TCI Europe

Tel: 320-37350700
Fax: +32 (0)37350701
Email: sales@tcieurope.eu
Country: Europe
ProdList: 23671
Advantage: 75

ecochem international chemical broker

Tel: --
Fax: --
Email: export@ecochem.dk
Country: Europe
ProdList: 6371
Advantage: 66

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View Lastest Price from (1S)-(-)-CAMPHORSULFONYLIMINE manufacturers

Career Henan Chemical Co

Product: (1S)-(-)-CAMPHORSULFONYLIMINE 60886-80-8
Price: US $9.80/KG
Min. Order: 1g
Purity: ≥99%
Supply Ability: 100kg
Release date: 2020-01-08

60886-80-8, (1S)-(-)-CAMPHORSULFONYLIMINERelated Search:

N-ACETYL-(2S)-BORNANE 10,2-SULTAM (+)-10-CAMPHORSULFONIMINE (1S)-(-)-Camphorsulfonylimine, 98+% 2-Ethyl-1-hexanethiol (1S)-(-)-CAMPHORSULFONYLIMINE Ethanesulfonamide 3-METHYL-1-BUTANETHIOL 2-METHYL-1-BUTANETHIOL Isobutylmercaptan 1,1,3-TRIMETHYLCYCLOPENTANE 1-PENTANESULFONAMIDE 4-04-00-00045 (Beilstein Handbook Reference) 1-HEXANESULFONAMIDE PROPANE-1-SULFONAMIDE 2,2,3,3-TETRAMETHYLPENTANE 1-HEPTANESULFONAMIDE CYCLOHEXYLMETHYL MERCAPTAN (1S)-(-)-3-OXOCAMPHORSULFONYLIMINE 98+%

(7S)-(-)-10,10-DIMETHYL-3-THIA-4-AZATRICYCLO[5.2.1.01,5]DEC-4-ENE 3,3-DIOXIDE

(7S)-10,10-DIMETHYL-3-THIA-4-AZATRICYCLO[5.2.1.01,5]DEC-4-ENE-3,3-DIOXIDE

(7S)-(-)-10,10-DIMETHYL-5-THIA-4-AZATRICYCLO[5.2.1.0(3,7)]DEC-3-ENE-5,5-DIOXIDE

(3AS)-(-)-4,5,6,7-TETRAHYDRO-8,8-DIMETHYL-3H-3A,6-METHANO-2,1-BENZISOTHIAZOLE 2,2-DIOXIDE

(3AS)-4,5,6,7-TETRAHYDRO-8,8-DIMETHYL-3H-3A,6-METHANO-2,1-BENZISOTHIAZOLE-2,2-DIOXIDE

(-)-10-CAMPHORSULFONIMINE

(1S)-(-)-CAMPHORSULFONYLIMINE

(1S)-(-)-(10-CAMPHORSULFONYL)IMINE

3H-3a,6-Methano-2,1-benzisothiazole, 4,5,6,7-tetrahydro-8,8-dimethyl-, 2,2-dioxide, (3aS,6R)-

(1s)-(-)-10,10-dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]dec-4-ene 3,3-dioxide

D-(-)-CAMPHORSULFONYL IMINE

(7S)-10,10-dimethyl-5-thia-4-azatricyclo-(5.2.1.0

Bornanesultam

SCamphorsulfonylimine

(1S)-(-)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]dec-4-ene 3,3-dioxide, (3aS)-(-)-4,5,6,7-Tetrahydro-8,8-dimethyl-3H-3a,6-methano-2,1-benzisothiazole-2,2-dioxide

(1R,7S)-10,10-Dimethyl-5-thia-4-azatricyclo[5.2.1.03,7]deca-3-ene 5,5-dioxide

(IS)-(-)-Camphorsulfonylimine

(-)-10-Camphorsulfonylimine

(3aS,6R)-4,5,6,7-Tetrahydro-8,8-dimethyl-3H-3a,6-methano-2,1-benzisothiazole 2,2-dioxide

(7S)-(-)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.0(1,5)]dec-4-ene 3,3-Dioxide (3aS)-(-)-4,5,6,7-Tetrahydro-8,8-dimethyl-3H-3a,6-methano-2,1-benzisothiazole 2,2-Dioxide

D-(-)-CAMPHORSULFONYL IMINE FOR SYNTHESI

(3aS,6R)-8,8-DiMethyl-4,5,6,7-tetrahydro-3H-3a,6-Methanobenzo[c]isothiazole 2,2-dioxide

6,10-Dibenzyl-N,N'-dimethyl-N,N,N',N'-tetrakis(4-methylbenzyl)-1,4-dioxaspiro[4.5]decane-(2R,3R)-diylbis(methylammonium)Tetrafluoroborate[=(R,R)-TaDiAS-2nd]&gt

(-)-10-Camphorsulfonimine &gt

(S)-Benzyl-2-[4-(trifluoromethyl)phenyl]-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazolium Tetrafluoroborate &gt

97.0%(N)

(S)-(-)-10-Camphorsulfonylimine

(-)-10-Camphorsulfonimine

60886-80-8

Asymmetric Synthesis

Chiral Building Blocks

Terpenes

Bicyclic Monoterpenes

Organic Building Blocks

Sulfonimides/Sulfinimides

Sulfur & Selenium Compounds

Chiral Reagents

Bicyclic Monoterpenes

Biochemistry

Terpenes

Chiral Compound

Intermediates & Fine Chemicals

Pharmaceuticals