Diphenylpiperidin-4-ylmethanol hydrochloride

Diphenylpiperidin-4-ylmethanol hydrochloride Basic information
Product Name:Diphenylpiperidin-4-ylmethanol hydrochloride
Synonyms:AZACYCLONOL HYDROCHLORIDE;DIPHENYL-PIPERIDIN-4-YL-METHANOLHYDROCHLORIDE;ALPHA,ALPHA-DIPHENYL-4-PIPERIDINOMETHANOL, HYDROCHLORIDE;alpha-(4-piperidyl)benzhydrolhydrochloride;alpha,alpha-diphenyl-4-piperidinemethanohydrochloride;alpha,alpha-diphenyl-4-piperidinemethanolhydrochloride;frenquelhydrochloride;gamma-pipradolhydrochloride
CAS:1798-50-1
MF:C18H22ClNO
MW:303.83
EINECS:217-284-9
Product Categories:
Mol File:1798-50-1.mol
Diphenylpiperidin-4-ylmethanol hydrochloride Structure
Diphenylpiperidin-4-ylmethanol hydrochloride Chemical Properties
Melting point 270-281 °C
form Crystalline Powder
color White to off-white
CAS DataBase Reference1798-50-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,T
Risk Statements 36/37/38-25
Safety Statements 24/25-45
HazardClass IRRITANT
HS Code 29333999
MSDS Information
ProviderLanguage
ACROS English
Diphenylpiperidin-4-ylmethanol hydrochloride Usage And Synthesis
Chemical Propertieswhite to off-white crystalline powder
OriginatorFrenquel,Merrell,US,1955
Manufacturing ProcessA mixture of 26 g (0.1 mol) of α-(4-pyridyl)-benzhydrol, 1.5 g of platinum oxide, and 250 ml of glacial acetic acid is shaken at 50-60°C under hydrogen at a pressure of 40-50 lb/in2. The hydrogenation is complete in 2 to 3 hours. The solution is filtered and the filtrate evaprated under reduced pressure. The residue is dissolved in a mixture of equal parts of methanol and butanone and 0.1 mol of concentrated hydrochloric acid is added. The mixture is cooled and filtered to give about 30 g of α-(4-piperidyl)benzhydrol hydrochloride, MP 283- 285°C, as a white, crystalline substance.
The free base is readily obtained from the hydrochloride salt by treatment with ammonia and when so obtained has a melting point of 160-161°C.
Brand nameFrenquel (Marion Merrell Dow).
Therapeutic FunctionTranquilizer
Diphenylpiperidin-4-ylmethanol hydrochloride Preparation Products And Raw materials
Raw materialsHydrogen
Fexofenadine hydrochloride FEXOFENADINE HYDROCHLORIDE 6-CHLORO-3-(3-(4-(HYDROXYDIPHENYLMETHYL)PIPERIDINE-1-CARBONYL)PIPERIDIN-1-YL)-4-PHENYLQUINOLIN-2(1H)-ONE alpha,alpha-Diphenyl-4-piperidinomethanol 7-(4-CHLOROBENZYL)-8-(4-(HYDROXYDIPHENYLMETHYL)PIPERIDIN-1-YL)-1,3-DIMETHYL-1H-PURINE-2,6(3H,7H)-DIONE Diphenoxylate 4-(ALPHA, ALPHA DIPHENYL) PIPERIDINE METHANOL HYDROCHLORIDE MONOHYDRATE Ethyl 4-{4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl}-alpha,alpha-dimethylbenzeneacetate hydrochloride Topotecan hydrochloride ETHYL 4-[4-4-(HYDROXYDIPHENYLMETHYL)-1-PIPERIDINYL-1-OXOBUTYL]-2,6-DIMETHYLBENZENEACETATE HYDROCHLOR A,A-DIMETHYL-4-[4-[4-(HYDROXYDIPHENYL METHYL)-1-PIPERIDINYL]-1-OXOBUTYL]PHENYL ACETIC ACID METHYL ESTER HYDROCHLORIDE 1,4-Benzenedimethanol Diphenylsilane Diphenylpiperidin-4-ylmethanol hydrochloride Donepezil Hydrochloride Methanol Loperamide hydrochloride tert-Butylchlorodiphenylsilane

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