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1-Propanol, 3-(trimethylsilyl)-, carbamate

Base Information Edit
  • Chemical Name:1-Propanol, 3-(trimethylsilyl)-, carbamate
  • CAS No.:3124-35-4
  • Molecular Formula:C7H17NO2Si
  • Molecular Weight:175.303
  • Hs Code.:
  • NSC Number:92692
  • DSSTox Substance ID:DTXSID50185159
  • Nikkaji Number:J69.785K
  • Wikidata:Q83056141
  • Mol file:3124-35-4.mol
1-Propanol, 3-(trimethylsilyl)-, carbamate

Synonyms:3-(trimethylsilyl)propyl carbamate;1-Propanol, 3-(trimethylsilyl)-, carbamate;3124-35-4;3-(Trimethylsilyl)-1-propanol carbamate;Carbamic acid, 3-(trimethylsilyl)propyl ester;BRN 2411130;3-(Trimethylsilyl)propyl ester of carbamic acid;NCIOpen2_001389;DTXSID50185159;NSC92692;NSC 92692;NSC-92692

Suppliers and Price of 1-Propanol, 3-(trimethylsilyl)-, carbamate
Supply Marketing:Edit
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
Total 2 raw suppliers
Chemical Property of 1-Propanol, 3-(trimethylsilyl)-, carbamate Edit
Chemical Property:
  • Vapor Pressure:0.0198mmHg at 25°C 
  • Boiling Point:252°Cat760mmHg 
  • Flash Point:106.2°C 
  • Density:0.937g/cm3 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:5
  • Exact Mass:175.102855319
  • Heavy Atom Count:11
  • Complexity:131
Purity/Quality:

99%min *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C[Si](C)(C)CCCOC(=O)N
Technology Process of 1-Propanol, 3-(trimethylsilyl)-, carbamate

There total 5 articles about 1-Propanol, 3-(trimethylsilyl)-, carbamate 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 2 steps
1: LiAlH4
2: (i) Py, (ii) liq. NH3
With lithium aluminium tetrahydride;
DOI:10.1021/jm00329a012
Guidance literature:
With trifluoroacetic acid; In benzene;
Refernces Edit
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