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

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Products Intro: Product Name:(1R)-(+)-2,10-Camphorsultam
CAS:108448-77-7
Purity:0.98 Package:25KG;5KG;1KG
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Products Intro: Product Name:(2S)-Bornane-10,2-sultam
CAS:108448-77-7
Purity:98%(Min,HPLC) Package:1G;1KG;100KG
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CAS:108448-77-7
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Products Intro: Product Name:(+)-Camphorsultam
CAS:108448-77-7
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Products Intro: Product Name:(2S)-Bornane-10,2-sultam
CAS:108448-77-7
Purity:98% Package:1KG;1USD

(2S)-Bornane-10,2-sultam manufacturers

(2S)-Bornane-10,2-sultam Basic information
Product Name:(2S)-Bornane-10,2-sultam
Synonyms: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
CAS:108448-77-7
MF:C10H17NO2S
MW:215.31
EINECS:
Product Categories:chiral;Asymmetric Synthesis;Bicyclic Monoterpenes;Biochemistry;Sulfur Compounds (for Synthesis);Synthetic Organic Chemistry;Terpenes;Peptide
Mol File:108448-77-7.mol
(2S)-Bornane-10,2-sultam Structure
(2S)-Bornane-10,2-sultam Chemical Properties
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
pka11.05±0.40(Predicted)
color White to Almost white
optical activity[α]20/D +32°, c = 5 in chloroform
BRN 4675755
InChIKeyDPJYJNYYDJOJNO-CFGJQEBVSA-N
CAS DataBase Reference108448-77-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
WGK Germany 3
HS Code 29242990
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
(2S)-Bornane-10,2-sultam Usage And Synthesis
Chemical Propertieswhite 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 MethodsThe (-)-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
Preparation Products(+)-10-CAMPHORSULFONIMINE
Tag:(2S)-Bornane-10,2-sultam(108448-77-7) Related Product Information
3-Aminobenzenesulfonamide N,N-Dimethylformamide Dacthal Dimethyl ether Dimethyl sulfoxide Methanesulfonamide Cyclopropanesulfonamide Dimethyl fumarate Sulfanilamide Benzenesulfonamide Dimethyl carbonate ETHANE Dimethyl sulfate Dimethyl phthalate Dimethyl disulfide p-Toluenesulfonamide (2R)-Bornane-10,2-sultam (1S)-(+)-10-CAMPHORSULFONAMIDE