(2S)-Bornane-10,2-sultam
- CAS No.
- 108448-77-7
- Chemical Name:
- (2S)-Bornane-10,2-sultam
- Synonyms
- (7aS)-8,8-Dimethylhexahydro-1H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide;2-sultaM;L-SultaM;(2S)-Bornane-10;L-2,10-amphorsultam;D-(-)-CAMPHOR SULTAM;(+)-10,2-CAMPHORSULTAM;(+)-2,10-CAMPHORSULTAM;(1R)-(+)-Camphorsultam;(2S)-Borne-10,2-sultam
- CBNumber:
- CB2411257
- Molecular Formula:
- C10H17NO2S
- Molecular Weight:
- 215.31
- MOL File:
- 108448-77-7.mol
- MSDS File:
- SDS
- Modify Date:
- 2024/8/29 17:54:30
| Melting point | 185-187 °C(lit.) |
|---|---|
| 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 | almost transparency in Chloroform |
| form | powder to crystal |
| pka | 11.05±0.40(Predicted) |
| color | White to Almost white |
| optical activity | [α]20/D +32°, c = 5 in chloroform |
| BRN | 4675755 |
| InChIKey | DPJYJNYYDJOJNO-CFGJQEBVSA-N |
| CAS DataBase Reference | 108448-77-7(CAS DataBase Reference) |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS07 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Warning | |||||||||
| Hazard statements | H315-H319-H335 | |||||||||
| Precautionary statements | P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P280a-P304+P340-P405-P501a-P261-P305+P351+P338 | |||||||||
| Hazard Codes | Xi | |||||||||
| Risk Statements | 36/37/38 | |||||||||
| Safety Statements | 26-36-37/39 | |||||||||
| WGK Germany | 3 | |||||||||
| HS Code | 29242990 | |||||||||
| NFPA 704 |
|
(2S)-Bornane-10,2-sultam Chemical Properties,Uses,Production
Chemical Properties
white to light yellow crystal powde
Uses
(1R)-(+)-2,10-Camphorsultam has been used as a reactant in the synthesis of pyrrolidine acid analogs as potent dual PPARα/γ agonists.
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.]
(2S)-Bornane-10,2-sultam Preparation Products And Raw materials
Global( 269)Suppliers
| Supplier | Tel | Country | ProdList | Advantage | Inquiry |
|---|---|---|---|---|---|
| CHEMSWORTH | +91-261-2397244 | New Delhi, India | 6707 | 30 | Inquiry |
| TCI Chemicals (India) Pvt. Ltd. | 1800 425 7889 | New Delhi, India | 6778 | 58 | Inquiry |
| A.J Chemicals | 91-9810153283 | New Delhi, India | 6124 | 58 | Inquiry |
| Reax Chemicals | 08048372701Ext 416 | Hyderabad, India | 4223 | 58 | Inquiry |
| Souvenier Chemicals | 08048372762Ext 645 | Mumbai, India | 396 | 58 | Inquiry |
| Biopharmacule Speciality Chemicals P Ltd (India) | +91 40 6462 1866 | Hyderabad, India | 526 | 58 | Inquiry |
| Keminntek Laboratories | 08048372631Ext 196 | Hyderabad, India | 209 | 58 | Inquiry |
| Clearsynth Labs | 91-22-45045900 | Maharashtra, India | 3889 | 58 | Inquiry |
| Changzhou Chontech Baocheng Chemical Co.,Ltd | +86-51982698291; +undefined15295095616 | China | 73 | 58 | Inquiry |
| Zibo Hangyu Biotechnology Development Co., Ltd | +86-0533-2185556 +8617865335152 | China | 10991 | 58 | Inquiry |
108448-77-7((2S)-Bornane-10,2-sultam)Related Search:
chevron_left
1of4
chevron_right
L-2,10-Camphorsultam,99%e.e.
(2S)-BORNANE-10,2-SULTAM
(1R)-(+)-2,10-CAMPHORSULTAM
(1R)-2,10-CAMPHORSULTAM
(1R,2S)-(+)-2,10-CAMPHORSULTAM
(1R,5S)-10,10-DIMETHYL-3-THIA-4-AZATRICYCLO[5.2.1.01,5]DECANE 3,3-DIOXIDE
(+)-2,10-CAMPHORSULTAM
(+)-10,2-CAMPHORSULTAM
(IR)-(+)-2,10-Camphorsultam
(1R)-(+)-2,10-camphorsultam ,98%
L-2,10-amphorsultam
(2S)-Bornane-10
2-sultaM
(2S)-Bornane-1,2-sultaM
L-SultaM
(2S)-Bornane-10,2-sultam
(1R,5S)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.0(1,5)]decane 3,3-Dioxide
(1R)-(+)-2,10-Camphorsultam
(5S,7S)-10,10-dimethyl-3λ-thia-4-azatricyclo[5.2.1.01,]decane-3,3-dione
(2S)-Bornane-10,2-sultam
(1R)-(+)-2,10-Camphorsultam
[3AR-(3A-ALPHA,6-ALPHA,7A-BETA)]-HEXAHYDRO-8,8-DIMETHYL-2,2-DIOXIDE-3H-3A,6-METHANO-2,1-BENZISOTHIAZOLE
[3aR-(3aalpha,6alpha,7abeta)]-Hexahydro-8,8-dimethyl-2,2-dioxide-3H-3a,6-methano-2,1-benzisothiazole
(+)-EXO-10,2-BORNANESULTAM
(+)-L-2,10-CAMPHORSULTAM
L(+)-10,2-CAMPHORSULTAME
D-(-)-CAMPHOR SULTAM
(+)-2,10-CAMPHORSULTAM 99%
(2S)-Bornane-10,2-sultam,99+%, (99+% ee)
(2S)-Bornane-10,2-sultam,98%
(+)-exo-10,2-Bornanesultam, (1R,5S)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]decane 3,3-dioxide
(+)-10,2-Camphorsultam, (+)-exo-10,2-Bornanesultam, L-2,10-Camphorsultam, (1R,5S)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]decane 3,3-dioxide
(1β,5α,7β)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]decane3,3-dioxide
(3aR)-1,4,5,6,7,7aβ-Hexahydro-8,8-dimethyl-3H-3aα,6α-methano-2,1-benzisothiazole 2,2-dioxide
(3aR,3aα,6α,7aβ)-8,8-Dimethyl-3a,6-methanooctahydro-2,1-benzisothiazole 2,2-dioxide
[3aR,7aβ,(+)]-Hexahydro-8,8-dimethyl-3H-3aα,6α-methano-2,1-benzisothiazole 2,2-dioxide
(1R)-(+)-Camphorsultam
(1R,2S)-(+)-10,2-Camphorsultam
(2S)-Borne-10,2-sultam
(1R,2S)-(+)-10,2-CamphorsuL
3H-3a,6-Methano-2,1-benzisothiazole, hexahydro-8,8-dimethyl-, 2,2-dioxide, (3aR,6S,7aS)-
(3aR)-8,8-dimethylhexahydro-2H-3a,6-methanobenzo[d]isothiazole 1,1-dioxide
(2S)-Bornane-10,2-sultam ISO 9001：2015 REACH
(3aR,6S,7aS)-8,8-Dimethylhexahydro-1H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide
(7aS)-8,8-Dimethylhexahydro-1H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide
(+)-10，2-Camphorsultam
(5S,7S)-10,10-dimethyl-3λ?-thia-4-azatricyclo[5.2.1.01?]decane 3,3-dioxide
(+)-2,10-Camphorsultam
108448-77-7
C10H17NO2S
Sulfur-Based
Sulfur Compounds (for Synthesis)
Bicyclic Monoterpenes
Terpenes
Asymmetric Synthesis
Chiral Auxiliaries
chiral
Asymmetric Synthesis
Bicyclic Monoterpenes
Biochemistry