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

Product Name
(N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM
CAS No.
94668-55-0
Chemical Name
(N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM
Synonyms
(1S)-N-crotyl-2,10-camphorsultam;(N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM;(R)-(-)-(2-BUTENOYL)-2,10-CAMPHORSULTAM;1-((7AR)-8,8-dimethyl-1,1-dioxidohexahydro-4H-3a,6-methanobenzo[d]isothiazol-7-yl)but-2-en-1-one;(E)-1-((3aS,6R,7aR)-8,8-Dimethyl-2,2-dioxidohexahydro-1H-3a,6-methanobenzo[c]isothiazol-1-yl)but-2-en-1-one;2-Buten-1-one, 1-[(3aS,6R,7aR)-tetrahydro-8,8-dimethyl-2,2-dioxido-3H-3a,6-methano-2,1-benzisothiazol-1(4H)-yl]-, (2E)-;(N-Crotonyl)-(2R)-bornane-10,2-sultam, (2E)-1-[(3aS,6R,7aR)-Tetrahydro-8,8-dimethyl-2,2-dioxido-3H-3a,6-methano-2,1-benzisothiazol-1(4H)-yl]-2-buten-1-one
CBNumber
CB2263324
Molecular Formula
C14H21NO3S
Formula Weight
283.39
MOL File
94668-55-0.mol
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(N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM Property

Melting point:
180-184 °C(lit.)
Boiling point:
397.2±25.0 °C(Predicted)
Density 
1.27±0.1 g/cm3(Predicted)
pka
-14.19±0.40(Predicted)
optical activity
[α]24/D 100°, c = 1 in ethanol
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
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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.

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

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
CCH0007016
Product name
(N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM
Purity
95.00%
Packaging
5MG
Price
$505.98
Updated
2021/12/16
Crysdot
Product number
CD11006222
Product name
(R)-(-)-(2-Butenoyl)-2,10-camphorsultam
Purity
97%
Packaging
1g
Price
$142
Updated
2021/12/16
Crysdot
Product number
CD11006222
Product name
(R)-(-)-(2-Butenoyl)-2,10-camphorsultam
Purity
97%
Packaging
5g
Price
$454
Updated
2021/12/16
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(N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM Chemical Properties,Usage,Production

Uses

(R)-(-)-(2-Butenoyl)-2,10-camphorsultam can be used:

  • In the asymmetric total synthesis of lycopodine via diastereoselective cyclization and intramolecular Mannich cyclization.
  • To prepare (S)-4,4-dichloro-3-methylbutanoic acid, which is utilized as a key intermediate for the total synthesis of dysideaproline E.

(N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM Preparation Products And Raw materials

Raw materials

Preparation Products

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(N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM Suppliers

China 28 France 1 Switzerland 1 United States 3 Global 33
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
52925
Advantage
58
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
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View Lastest Price from (N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM manufacturers

Career Henan Chemical Co
Product
(N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM 94668-55-0
Price
US $1.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
20KG
Release date
2018-08-07

94668-55-0, (N-CROTONYL)-(2R)-BORNANE-10,2-SULTAMRelated Search:

N-PROPIONYL-(2S)-BORNANE- 10,2-SULTAM (N-Acetyl)-(2S)-bornane-10,2-sultaM (1S)-(+)-(Camphorylsulfonyl)oxaziridine (2S)-Bornane-10,2-sultam (+)-10-CAMPHORSULFONIMINE (R)-(-)-(2-Methylacryloyl)-2,10-camphorsultam (N-CROTONYL)-(2S)-BORNANE-10,2-SULTAM (S)-(+)-(2-Methylacryloyl)-2,10-camphorsultam N-ACETYL-(2S)-BORNANE 10,2-SULTAM (2R)-Bornane-10,2-sultam BORNYLAMINE ALLYLCYCLOHEXYLAMINE (N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM N-Methyl 1,1-dioxo-isothiazolidine N-CYCLOHEXYLACRYLAMIDE N-ALLYLCYCLOPENTYLAMINE N-ETHYL 1,1-DIOXO-ISOTHIAZOLIDINE ISOTHIAZOLINE 1,1-DIOXIDE

  • (R)-(-)-(2-BUTENOYL)-2,10-CAMPHORSULTAM
  • (N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM
  • (N-Crotonyl)-(2R)-bornane-10,2-sultam, (2E)-1-[(3aS,6R,7aR)-Tetrahydro-8,8-dimethyl-2,2-dioxido-3H-3a,6-methano-2,1-benzisothiazol-1(4H)-yl]-2-buten-1-one
  • (1S)-N-crotyl-2,10-camphorsultam
  • 2-Buten-1-one, 1-[(3aS,6R,7aR)-tetrahydro-8,8-dimethyl-2,2-dioxido-3H-3a,6-methano-2,1-benzisothiazol-1(4H)-yl]-, (2E)-
  • (E)-1-((3aS,6R,7aR)-8,8-Dimethyl-2,2-dioxidohexahydro-1H-3a,6-methanobenzo[c]isothiazol-1-yl)but-2-en-1-one
  • 1-((7AR)-8,8-dimethyl-1,1-dioxidohexahydro-4H-3a,6-methanobenzo[d]isothiazol-7-yl)but-2-en-1-one
  • 94668-55-0
  • C14H21NSO3
  • Sulfur-Based
  • Chiral Auxiliaries
  • Asymmetric Synthesis
  • Peptide