Alimadol

Alimadol Suppliers list
Company Name: Hubei Jusheng Technology Co.,Ltd.
Tel: 18871490254
Email: linda@hubeijusheng.com
Products Intro: Product Name:3-methoxy-3,3-diphenyl-N-prop-2-enylpropan-1-amine
CAS:52742-40-2
Purity:0.99 Package:5KG;1KG
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:Alimadol;A 4020;A4020;A-4020
CAS:52742-40-2
Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: TargetMol Chemicals Inc.  
Tel: 4008200310
Email: marketing@tsbiochem.com
Products Intro: Product Name:Alimadol;Alimadol
CAS:52742-40-2
Purity:98% Package:5 mg
Company Name: Lanospharma Laboratories Co.,Ltd  
Tel: 13440048448
Email: sales@lanospharma.com
Products Intro:
Alimadol Basic information
Product Name:Alimadol
Synonyms:Alimadol;3-Methoxy-3,3-diphenyl-N-(2-propenyl)-1-propanamine;1,1-diphenyl-1-methoxy-3-allylaminopropane;3-methoxy-3,3-diphenyl-N-prop-2-enylpropan-1-amine;Benzenepropanamine, γ-methoxy-γ-phenyl-N-2-propen-1-yl-;A 4020;A4020;A-4020
CAS:52742-40-2
MF:C19H23NO
MW:281.39
EINECS:
Product Categories:
Mol File:52742-40-2.mol
Alimadol Structure
Alimadol Chemical Properties
Boiling point 404.8±45.0 °C(Predicted)
density 1.008±0.06 g/cm3(Predicted)
pka9.53±0.19(Predicted)
Safety Information
MSDS Information
Alimadol Usage And Synthesis
OriginatorAlimadol ,ZYF Pharm Chemical
Manufacturing Process12 g 3,3-diphenyl-3-methoxypropylamine, 13.5 g trifluoroacetic acid anhydride, 6.0 g pyridine and 100 ml benzene was heated by stirring for 1 hour at 40°C. Then in was cooled to 0°C and poured in water. The organic layer was separated, washed with diluted HCl and water, and evaporated to dryness. The residue N-(3,3-diphenyl-3-methoxypropyl)trifluoroacetamide melted at 108°-110°C. Yield: 98%.
8 g above amide was in 80 ml hexamethyl phosphoric acid amide dissolved mixed with 1.7 g sodium hydride and stirred for 3 hours. Then 5.7 g allyl bromide was added dropwise and the mixture was stirred for 30 minutes. It was diluted with water and extracted with benzene. Benzene layer was separated, evaporated to dryness. The residue was mixed with 100 ml of 75% ethanol and 1 g sodium hydroxide and heated for 1 hour. Ethanol was distilled off and reaction product was extracted with ether. Yield of N-(3-methoxy-3,3- diphenylpropyl)allylamin (or 1,1-diphenyl-1-methoxy-3-allylaminopropane) was 6.5 g (97%). MP: 40°-50°C. Hydrochloride melted at 137°-138°C.
Therapeutic FunctionAnalgesic
Alimadol Preparation Products And Raw materials
Raw materialsAllyl bromide-->Trifluoroacetic anhydride
Tag:Alimadol(52742-40-2) Related Product Information
Alimadol