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Hexahydrosiladifenidol

Base Information
  • Chemical Name:Hexahydrosiladifenidol
  • CAS No.:98299-40-2
  • Molecular Formula:C20H33 N O Si
  • Molecular Weight:331.574
  • Hs Code.:2933399090
  • European Community (EC) Number:635-538-0
  • UNII:LXZ2G00X0W
  • DSSTox Substance ID:DTXSID20913340
  • Nikkaji Number:J128.591B
  • Wikidata:Q27077980
  • Pharos Ligand ID:SZYDA6B72CPT
  • ChEMBL ID:CHEMBL3545990
  • Mol file:98299-40-2.mol
Hexahydrosiladifenidol

Synonyms:hexahydro-sila-diphenidol;hexahydrosiladifenidol;hexahydrosiladiphenidol;HHSi-difenidol;HHSiD

Suppliers and Price of Hexahydrosiladifenidol
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
  • American Custom Chemicals Corporation
  • HHID 95.00%
  • 5MG
  • $ 504.87
Total 4 raw suppliers
Chemical Property of Hexahydrosiladifenidol
Chemical Property:
  • Vapor Pressure:7.14E-09mmHg at 25°C 
  • Boiling Point:449.7°Cat760mmHg 
  • PKA:13.91±0.20(Predicted) 
  • Flash Point:225.8°C 
  • PSA:23.47000 
  • Density:1.03g/cm3 
  • LogP:3.97960 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:6
  • Exact Mass:331.233141211
  • Heavy Atom Count:23
  • Complexity:333
Purity/Quality:

97% *data from raw suppliers

HHID 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xn 
  • Hazard Codes:Xn 
  • Statements: 20/21/22 
  • Safety Statements: 36 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CCC(CC1)[Si](CCCN2CCCCC2)(C3=CC=CC=C3)O
Technology Process of Hexahydrosiladifenidol

There total 6 articles about Hexahydrosiladifenidol 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:
With hydrogenchloride; In isopropyl alcohol; for 16h; Yield given; Ambient temperature;
DOI:10.1002/jlac.198519851112
Guidance literature:
Multi-step reaction with 2 steps
1: 96 percent / methanol / 16 h / Heating
2: 0.5N HCl / propan-2-ol / 16 h / Ambient temperature
With hydrogenchloride; In methanol; isopropyl alcohol;
DOI:10.1002/jlac.198519851112
Guidance literature:
Multi-step reaction with 4 steps
1: 71 percent / diethyl ether / 1.) 15h, room temperature, 2.) 4h, reflux
2: 87 percent / benzene; diethyl ether / 4 h / Heating
3: 96 percent / methanol / 16 h / Heating
4: 0.5N HCl / propan-2-ol / 16 h / Ambient temperature
With hydrogenchloride; In methanol; diethyl ether; isopropyl alcohol; benzene;
DOI:10.1002/jlac.198519851112
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