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Cyclohexanepropanoic acid, alpha-amino-2-(2-phosphonoethyl)-

Base Information Edit
  • Chemical Name:Cyclohexanepropanoic acid, alpha-amino-2-(2-phosphonoethyl)-
  • CAS No.:117571-54-7
  • Molecular Formula:C11H22NO5P
  • Molecular Weight:279.273
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40922459
  • Nikkaji Number:J365.974G
  • ChEMBL ID:CHEMBL322304
  • Mol file:117571-54-7.mol
Cyclohexanepropanoic acid, alpha-amino-2-(2-phosphonoethyl)-

Synonyms:2-amino-4,5-(1,2-cyclohexyl)-7-phosphonoheptanoic acid;GPI 3000;GPI-3000;NPC 12626;NPC 17742;NPC-12626;NPC-17742

Suppliers and Price of Cyclohexanepropanoic acid, alpha-amino-2-(2-phosphonoethyl)-
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 1 raw suppliers
Chemical Property of Cyclohexanepropanoic acid, alpha-amino-2-(2-phosphonoethyl)- Edit
Chemical Property:
  • Vapor Pressure:3.33E-12mmHg at 25°C 
  • Boiling Point:519.9°Cat760mmHg 
  • Flash Point:268.2°C 
  • Density:1.293g/cm3 
  • XLogP3:-2
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:6
  • Exact Mass:279.12355980
  • Heavy Atom Count:18
  • Complexity:329
Purity/Quality:

99%min *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CCC(C(C1)CCP(=O)(O)O)CC(C(=O)O)N
Technology Process of Cyclohexanepropanoic acid, alpha-amino-2-(2-phosphonoethyl)-

There total 42 articles about Cyclohexanepropanoic acid, alpha-amino-2-(2-phosphonoethyl)- 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; at 95 ℃; for 48h;
DOI:10.1021/jo00077a058
Guidance literature:
Multi-step reaction with 9 steps
1: 78 percent / LiEt3BH / tetrahydrofuran / Ambient temperature
2: DIBAL / toluene / 1 h / -45 - -35 °C
3: NaH / tetrahydrofuran; toluene / 1.) r.t., 1 h, 2.) 0 deg C, 30 min; 60 deg C, 4 h
4: 88 percent / pyridine-SO3, Et3N / dimethylsulfoxide / 4 h / Ambient temperature
5: 70 percent / LiOH*H2O / aq. ethanol / 0 deg C, 1 h; r.t., 2 h
6: 95 percent / H2 / Raney nickel / methanol / 48 h / 65 °C / 25857.4 Torr
7: D-hydantoinase
8: 70 percent / NaNO2, aq. HCl
9: 100 percent / 10N aq. HCl / 48 h / 95 °C
With hydrogenchloride; lithium hydroxide; D-hydantoinase; hydrogen; sulfur trioxide pyridine complex; sodium hydride; diisobutylaluminium hydride; lithium triethylborohydride; triethylamine; sodium nitrite; nickel; In tetrahydrofuran; methanol; ethanol; dimethyl sulfoxide; toluene;
DOI:10.1021/jo00077a058
Guidance literature:
Multi-step reaction with 8 steps
1: DIBAL / toluene / 1 h / -45 - -35 °C
2: NaH / tetrahydrofuran; toluene / 1.) r.t., 1 h, 2.) 0 deg C, 30 min; 60 deg C, 4 h
3: 88 percent / pyridine-SO3, Et3N / dimethylsulfoxide / 4 h / Ambient temperature
4: 70 percent / LiOH*H2O / aq. ethanol / 0 deg C, 1 h; r.t., 2 h
5: 95 percent / H2 / Raney nickel / methanol / 48 h / 65 °C / 25857.4 Torr
6: D-hydantoinase
7: 70 percent / NaNO2, aq. HCl
8: 100 percent / 10N aq. HCl / 48 h / 95 °C
With hydrogenchloride; lithium hydroxide; D-hydantoinase; hydrogen; sulfur trioxide pyridine complex; sodium hydride; diisobutylaluminium hydride; triethylamine; sodium nitrite; nickel; In tetrahydrofuran; methanol; ethanol; dimethyl sulfoxide; toluene;
DOI:10.1021/jo00077a058
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