(1S)-(-)-10-Mercaptoisoborneol

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(1S)-(-)-10-Mercaptoisoborneol Basic information
Uses
Product Name:(1S)-(-)-10-Mercaptoisoborneol
Synonyms:Mercaptoisoborneol;(1S)-(-)-10-MERCAPTOISOBORNEOL 98+%;(-)-10-Mercaptoisoborneol;(+)-10-Mercaptoisoborneol;(1S,2R,4R)-1-(Mercaptomethyl)-7,7-dimethylbicyclo[2.2.1]heptane-2-ol;(1S,4R)-6β-Hydroxybornane-10-thiol;(4α)-1β-(Mercaptomethyl)-7,7-dimethylbicyclo[2.2.1]heptane-2α-ol;[1S,4α,(-)]-2α-Hydroxy-7,7-dimethylbicyclo[2.2.1]heptane-1β-methanethiol
CAS:71242-58-5
MF:C10H18OS
MW:186.32
EINECS:
Product Categories:Asymmetric Synthesis;Bicyclic Monoterpenes;Biochemistry;Synthetic Organic Chemistry;Terpenes
Mol File:71242-58-5.mol
(1S)-(-)-10-Mercaptoisoborneol Structure
(1S)-(-)-10-Mercaptoisoborneol Chemical Properties
Melting point 72 °C
Boiling point 270.401±13.00 °C(Press: 760.00 Torr)(predicted)
density 1.093±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
solubility almost transparency in Chloroform
pka10.482±0.10(predicted)
form powder to crystal
color White to Almost white
Safety Information
HS Code 2930909899
MSDS Information
(1S)-(-)-10-Mercaptoisoborneol Usage And Synthesis
Uses(1S)-(-)-10-mercaptoisoborneol is a camphor derivative. It can be prepared from (+)-10-camphor sulfonyl chloride as a raw material, first by preparing (1S)-10-mercaptocamphor, and then reducing the carbonyl group to obtain (1S)-(-)-10-mercaptoisoborneol.
(1S)-(-)-10-Mercaptoisoborneol Preparation Products And Raw materials
Tag:(1S)-(-)-10-Mercaptoisoborneol(71242-58-5) Related Product Information
DL-Isoborneol L-1-Phenylethylamine (1S)-(-)-10-Mercaptoisoborneol (+)-N,N-Dicyclohexyl-(1R)-isoborneol-10-sulfonamide Borneol oil (S)-Camphorsulfonic acid diisopropylamide dimethyl acetal