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2-Hydroxymethyl Olanzapine

Base Information
  • Chemical Name:2-Hydroxymethyl Olanzapine
  • CAS No.:174756-45-7
  • Molecular Formula:C17H20N4OS
  • Molecular Weight:328.438
  • Hs Code.:
  • Mol file:174756-45-7.mol
2-Hydroxymethyl Olanzapine

Synonyms:LY 290411

Suppliers and Price of 2-Hydroxymethyl Olanzapine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 2-HydroxymethylOlanzapine
  • 25mg
  • $ 3025.00
  • TRC
  • 2-HydroxymethylOlanzapine
  • 1mg
  • $ 185.00
  • Medical Isotopes, Inc.
  • 2-HydroxymethylOlanzapine-d3(Major)
  • 1 mg
  • $ 725.00
  • American Custom Chemicals Corporation
  • 2-HYDROXY METHYL OLANZAPINE 95.00%
  • 10MG
  • $ 1963.50
Total 13 raw suppliers
Chemical Property of 2-Hydroxymethyl Olanzapine
Chemical Property:
  • Vapor Pressure:4.3E-12mmHg at 25°C 
  • Melting Point:210-212?C 
  • Boiling Point:530.7°C at 760 mmHg 
  • Flash Point:274.8°C 
  • PSA:79.34000 
  • Density:1.4g/cm3 
  • LogP:2.07250 
  • Storage Temp.:-20°C Freezer, Under Inert Atmosphere 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly) 
Purity/Quality:

99%, *data from raw suppliers

2-HydroxymethylOlanzapine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses A minor metabolite of Olanzapine. A minor metabolite of Olanzapine A minor labelled metabolite of Olanzapine
Technology Process of 2-Hydroxymethyl Olanzapine

There total 7 articles about 2-Hydroxymethyl Olanzapine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 5 steps
1: LiOH / dimethylsulfoxide
2: POCl3
3: SnCl2, aq. HCl / ethanol
4: NaBH4 / ethanol
5: toluene; dimethylsulfoxide / Heating
With hydrogenchloride; lithium hydroxide; sodium tetrahydroborate; tin(ll) chloride; trichlorophosphate; In ethanol; dimethyl sulfoxide; toluene;
DOI:10.1016/S0960-894X(96)00567-7
Guidance literature:
Multi-step reaction with 5 steps
1: LiOH / dimethylsulfoxide
2: POCl3
3: SnCl2, aq. HCl / ethanol
4: NaBH4 / ethanol
5: toluene; dimethylsulfoxide / Heating
With hydrogenchloride; lithium hydroxide; sodium tetrahydroborate; tin(ll) chloride; trichlorophosphate; In ethanol; dimethyl sulfoxide; toluene;
DOI:10.1016/S0960-894X(96)00567-7
Guidance literature:
Multi-step reaction with 4 steps
1: POCl3
2: SnCl2, aq. HCl / ethanol
3: NaBH4 / ethanol
4: toluene; dimethylsulfoxide / Heating
With hydrogenchloride; sodium tetrahydroborate; tin(ll) chloride; trichlorophosphate; In ethanol; dimethyl sulfoxide; toluene;
DOI:10.1016/S0960-894X(96)00567-7
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