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CAS NO.41274-09-3
(R)-Glycerol 1-(p-toluenesulfonate) Basic information |
Product Name: | (R)-Glycerol 1-(p-toluenesulfonate) |
Synonyms: | (R)-GLYCEROL 1-(P-TOLUENESULFONATE);SN-GLYCEROL 1-(P-TOLUENESULFONATE);SN-GLYCERYL 1-(P-TOLUENESULFONATE);(R)-1-TOSYL-GLYCEROL;(R)-1-TOSYLOXY-2,3-PROPANEDIOL;(R)-2,3-DIHYDROXYPROPYL P-TOLUENESULFONATE;(R)-3-TOSYLOXY-1,2-PROPANEDIOL;(R)-1-Toxyloxy-2,3-propanediol |
CAS: | 41274-09-3 |
MF: | C10H14O5S |
MW: | 246.28 |
EINECS: | |
Product Categories: | chiral;Chiral Reagents;Aromatics;Sulfur & Selenium Compounds |
Mol File: | 41274-09-3.mol |
(R)-Glycerol 1-(p-toluenesulfonate) Chemical Properties |
mp | 54-59°C |
storage temp. | −20°C |
CAS DataBase Reference | 41274-09-3(CAS DataBase Reference) |
MSDS Information |
Provider | Language |
---|---|
SigmaAldrich | English |
(R)-Glycerol 1-(p-toluenesulfonate) Usage And Synthesis |
Usage | A chiral synthon for general asymmetric synthesis. An intermediate for the synthesis of chiral aryloxypropanolamines, which make up the majority of known potent beta-adrenergic blockers |
(R)-Glycerol 1-(p-toluenesulfonate) Preparation Products And Raw materials |
(R)-Glycerol 1-(p-toluenesulfonate) Basic information |
Product Name: | (R)-Glycerol 1-(p-toluenesulfonate) |
Synonyms: | (R)-GLYCEROL 1-(P-TOLUENESULFONATE);SN-GLYCEROL 1-(P-TOLUENESULFONATE);SN-GLYCERYL 1-(P-TOLUENESULFONATE);(R)-1-TOSYL-GLYCEROL;(R)-1-TOSYLOXY-2,3-PROPANEDIOL;(R)-2,3-DIHYDROXYPROPYL P-TOLUENESULFONATE;(R)-3-TOSYLOXY-1,2-PROPANEDIOL;(R)-1-Toxyloxy-2,3-propanediol |
CAS: | 41274-09-3 |
MF: | C10H14O5S |
MW: | 246.28 |
EINECS: | |
Product Categories: | chiral;Chiral Reagents;Aromatics;Sulfur & Selenium Compounds |
Mol File: | 41274-09-3.mol |
(R)-Glycerol 1-(p-toluenesulfonate) Chemical Properties |
mp | 54-59°C |
storage temp. | −20°C |
CAS DataBase Reference | 41274-09-3(CAS DataBase Reference) |
MSDS Information |
Provider | Language |
---|---|
SigmaAldrich | English |
(R)-Glycerol 1-(p-toluenesulfonate) Usage And Synthesis |
Usage | A chiral synthon for general asymmetric synthesis. An intermediate for the synthesis of chiral aryloxypropanolamines, which make up the majority of known potent beta-adrenergic blockers |
(R)-Glycerol 1-(p-toluenesulfonate) Preparation Products And Raw materials |