(2R)-Bornane-10,2-sultam

Product Name: (2R)-Bornane-10,2-sultam
CAS No.: 94594-90-8
Chemical Name: (2R)-Bornane-10,2-sultam
Synonyms: D-SultaM;(1S,2R)-(-)-;(2R)-Bornane-10;L-(+)-CAMPHOR SULTAM;(2R)-Bornane-10,2-su;(-)-10,2-CAMPHORSULTAM;(1S)-(-)-Camphorsultam;(2R)-Borne-10,2-sultam;(-)-2,10-Camphorsultam;(1S)-2,10-CAMPHORSULTAM
CBNumber: CB9468760
Molecular Formula: C10H17NO2S
Formula Weight: 215.31
MOL File: 94594-90-8.mol

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(2R)-Bornane-10,2-sultam Property

Melting point:: 183-185 °C
alpha: -33 º (c=4.9, CHCl3)
Boiling point:: 324.8±25.0 °C(Predicted)
Density: 1.1469 (rough estimate)
refractive index: -31 ° (C=1, CHCl3)
storage temp.: Sealed in dry,Room Temperature
solubility: Chloroform, Ethanol, Methanol
form: Liquid
pka: 11.05±0.40(Predicted)
color: Clear colorless
optical activity: [α]19/D 32°, c = 5 in chloroform
Water Solubility: Slightly soluble in water.
BRN: 83811
CAS DataBase Reference: 94594-90-8(CAS DataBase Reference)
NIST Chemistry Reference: (-)-10,2-Camphorsultam(94594-90-8)

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Safety

Hazard Codes: Xi
Risk Statements: 36/37/38
Safety Statements: 26-37/39-36
WGK Germany: 3
HS Code: 29349990

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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.

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: 298352
Product name: (1S)-(?)-2,10-Camphorsultam
Purity: 98%
Packaging: 5g
Price: $94.2
Updated: 2024/03/01

TCI Chemical

Product number: C1325
Product name: (-)-10,2-Camphorsultam
Purity: >98.0%(GC)
Packaging: 1g
Price: $25
Updated: 2024/03/01

TCI Chemical

Product number: C1325
Product name: (-)-10,2-Camphorsultam
Purity: >98.0%(GC)
Packaging: 5g
Price: $64
Updated: 2024/03/01

Alfa Aesar

Product number: A15897
Product name: (1S,2R)-(-)-10,2-Camphorsultam, 99%
Packaging: 5g
Price: $196.65
Updated: 2024/03/01

Alfa Aesar

Product number: A15897
Product name: (1S,2R)-(-)-10,2-Camphorsultam, 99%
Packaging: 1g
Price: $68.5
Updated: 2021/12/16

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(2R)-Bornane-10,2-sultam Chemical Properties,Usage,Production

Chemical Properties

white to light yellow crystal powde

Uses

(1S,2R)-(-)-10,2-Camphorsultam is used in the asymmetric synthesis of (S)- and (R)-N-Fmoc-S-trityl-α-methylcysteine. It is used as proton source in the synthesis of chiral α,γ-substituted γ-butyrolactones. It is also employed as a chiral probe for the optical resolution by HPLC and X-ray crystallographic determination of the absolute stereochemistry of carboxylic acids. Also used to prepare N-acryloyl derivatives which are employed as dienophiles in asymmetric Diels-Alder reactions. and for other asymmetric transformations.

Uses

(1S)-(?)-2,10-Camphorsultam may be used in the asymmetric synthesis of (S)- and (R)-N-Fmoc-S-trityl-α-methylcysteine. It may be used as proton source in the synthesis of chiral α,γ-substituted γ-butyrolactones.

Uses

(2R)-Bornane-10,2-sultam is a reagent used to make Camphorsultam conjugates.

General Description

(1S,2R,4R)-(?)-2,10-Camphorsultam may be employed as a chiral probe for the optical resolution by HPLC and X-ray crystallographic determination of the absolute stereochemistry of carboxylic acids.

Purification Methods

The (-)-enantiomer is recrystallised from 95% EtOH and dried in a vacuum desiccator. It dissolves in dilute aqueous NaOH and can be precipitated without hydrolysis by acidifying. It forms the N-Na salt in EtOH (by addition of Na to the EtOH solution), and the salt can be methylated with MeI to give the (-)-N-Me lactam with m 80o after recrystallisation from hot H2O and has []D -59.6o (c 5, CHCl3) [Shriner et al. J Am Chem Soc 60 2794 1938]. [Oppolzer et al. Helv Chim Acta 69 1142 1986, Weismiller et al. Org Synth 69 154 1955, Beilstein 27 III/IV 1007.]

(2R)-Bornane-10,2-sultam Preparation Products And Raw materials

Raw materials

Preparation Products

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(2R)-Bornane-10,2-sultam Suppliers

Americas 1 Belgium 2 Canada 1 China 180 Europe 4 France 2 Germany 9 India 10 Italy 1 Japan 2 Poland 2 South Korea 1 Switzerland 4 The Netherlands 1 Ukraine 1 United Kingdom 14 United States 28 Global 263

Accela ChemBio Inc.

Tel: +1(858) 699-3322
Fax: +1(858) 876-1948
Email: marketing@accelachem.com
Country: United States
ProdList: 6027
Advantage: 65

Accela ChemBio Inc.

Tel: (+1)-858-699-3322
Fax: (+1)-858-876-1948
Email: info@accelachem.com
Country: United States
ProdList: 19965
Advantage: 58

Alchem Pharmtech,Inc.

Tel: 8485655694
Email: sales@alchempharmtech.com
Country: United States
ProdList: 63711
Advantage: 58

Aladdin Scientific

Tel: +1-833-552-7181
Email: sales@aladdinsci.com
Country: United States
ProdList: 57511
Advantage: 58

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View Lastest Price from (2R)-Bornane-10,2-sultam manufacturers

Hebei Saisier Technology Co., LTD

Product: (2R)-Bornane-10,2-sultam 94594-90-8
Price: US $6.00/KG
Min. Order: 1KG
Purity: More than 99%
Supply Ability: 2000KG/MONTH
Release date: 2024-04-24

Hebei Duling International Trade Co. LTD

Product: (-)-10,2-Camphorsultam 94594-90-8
Price: US $20.00/kg
Min. Order: 1kg
Purity: 99%
Supply Ability: 5000 tons
Release date: 2022-09-16

Shaanxi Dideu Medichem Co. Ltd

Product: (2R)-Bornane-10,2-sultam 94594-90-8
Price: US $0.00-0.00/KG
Min. Order: 1g
Purity: 99% HPLC
Supply Ability: 2000tons
Release date: 2019-12-30

94594-90-8, (2R)-Bornane-10,2-sultamRelated Search:

N-Acetylsulfanilyl chloride p-Toluenesulfonamide (1R)-(-)-10-Camphorsulfonic acid Dimethyl ether ETHANE Dimethyl phthalate Dimethyl sulfide Dimethyl fumarate Sulfanilamide N,N-Dimethylformamide (-)-CAMPHOR Benzenesulfonamide Dimethyl sulfoxide L(-)-10-Camphorsulfonyl chloride (1R,2R)-(-)-1,2-Diaminocyclohexane Ethyl (S)-9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylate 3-METHOXY-DL-TYROSINE L(-)-Carvone

(-)-EXO-10,2-BORNANESULTAM

(-)-D-2,10-CAMPHORSULTAM

(-)-D-2,10-CAMPHOSULTAM

D(-)-10,2-CAMPHORSULTAME

(2R)-BORNANE-10,2-SULTAM

(1S)-(-)-2,10-CAMPHORSULTAM

(1S)-2,10-CAMPHORSULTAM

(1S,2R)-(-)-2,10-CAMPHORSULTAM

(1S,5R)-10,10-DIMETHYL-3-THIA-4-AZATRICYCLO[5.2.1.0(1,5)]DECANE 3,3-DIOXIDE

(-)-10,2-CAMPHORSULTAM

[3AS-(3A-ALPHA,6-ALPHA,7A-BETA)]-HEXAHYDRO-8,8-DIMETHYL-2,2-DIOXIDE-3H-3A,6-METHANO-2,1-BENZISOTHIAZOLE

[3as-(3aalpha,6alpha,7abeta)]-hexahydro-8,8-dimethyl-2,2-dioxide-3h-3a,6-methano-2,1-benzisothiazole

[3AS-(3AALPHA,6ALPHA,7ABETA)]-HEXAHYDRO-8,8-DIMETHYL-3H-3A,6-METHANO-2,1-BENZISOTHIAZOLE-2,2-DIOXIDE

(1S)-(-)-Camphorsultam

(1S,2R)-(-)-10,2-Camphorsultam

(1S,2R)-(-)-2,10-CAMPHORSULTAME

3H-3a,6-Methano-2,1-benzisothiazole, hexahydro-8,8-dimethyl-, 2,2-dioxide, (3aS,6R,7aR)-

(-)-exo-10,2-Bornanesultam, (1S,5R)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]decane 3,3-dioxide

(-)-10,2-Camphorsultam, (-)-exo-10,2-Bornanesultam, [3aS-(3aα,6α,7aβ)]-hexahydro-8,8-dimethyl-3H-3a,6-methano-2,1-benzisothiazole-2,2-dioxide, (1S,5R)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]decane 3,3-dioxide

(2R)-10,2-Camphorsultam

(2R)-Bornane-10,2-sultam, 99+%, ee:>99%

D-(+)-CAMPHOR SULTAM INFRA-ACIDAMIDE

L-(+)-CAMPHOR SULTAM

(IS)-(-)-2,10-Camphorsultam

(2R)-Bornane-10,2-sultam ,98%

[3aS-(3aα,6α,7aβ)]-hexahydro-8,8-dimethyl-3H-3a,6-methano-2,1-benzisothiazole-2,2-dioxide

(2R)-Bornane-10,2-sultam99+%(>99% ee)

(3aR)-Hexahydro-8,8-dimethyl-3H-3aα,6α-methano-2,1-benzisothiazole 2,2-dioxide

(3aS)-1,3,5,6,7,7aα-Hexahydro-4H-3aβ,6β-isopropylidene-2,1-benzisothiazole 2,2-dioxide

(3aS)-1,4,5,6,7,7aα-Hexahydro-8,8-dimethyl-3H-3aβ,6β-methano-2,1-benzisothiazole 2,2-dioxide

(3aS,7aα)-8,8-Dimethyl-3aβ,6β-methanooctahydro-2,1-benzisothiazole 2,2-dioxide

(7aα)-8,8-Dimethyl-3aβ,6β-methanooctahydro-2,1-benzisothiazole 2,2-dioxide

[3aS,7aα,(-)]-Hexahydro-8,8-dimethyl-3H-3aβ,6β-methano-2,1-benzisothiazole 2,2-dioxide

(1S,2R)-(-)-

(2R)-Bornane-10,2-su

(2R)-Bornane-1,2-sultaM

(1S)-(-)-10,2-CaMphorsultaM

Hexahydro-8,8-diMethyl-3H-3a,6-Methano-2,1-benzisothiazole

D-SultaM

(2R)-Bornane-10,2-sultam (1S,5R)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.0(1,5)]decane 3,3-Dioxide

(2R)-Bornane-10,2-sultaM, 99+%

(1S,2R)-(-)-2,10-CAMPHORSULTAME FOR SYNT

(3aS,6S,7aS)-8,8-DiMethylhexahydro-1H-3a,6-Methanobenzo[c]isothiazole 2,2-dioxide

(2R)-Bornane-10,2-sultam (1S)-(-)-2,10-Camphorsultam

(1<i>S</i>)-(-)-2,10-Camphorsultam

(2R)-Borne-10,2-sultam

D-2,10-Camphorsultam,99%e.e.

(2R)-Bornane-10, 2-sultam, ≥99% ee

(-)-10,2-Camphorsultam &gt

(1S)-(?)-2,10-CamphorsuL

(-)-10,2-Camphorsultam?

(1S)-(-)-2,11-Camphorsultam

(2R)-Bornane-10,2-sultam ISO 9001：2015 REACH

(-)-2,10-Camphorsultam

(1S,2R)-(-)-10,2-Camphorsultam, 99%,

(5R,7R)-10,10-dimethyl-3thia-4-azatricyclo[5.2.1.01?]decane 3,3-dioxide

(3aS,6R,7aR)-8,8-Dimethylhexahydro-1H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide

(2R)-Bornane-10