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(3S)-3-amino-2-hydroxy-5-methylhexanoic acid;hydrochloride

Base Information
  • Chemical Name:(3S)-3-amino-2-hydroxy-5-methylhexanoic acid;hydrochloride
  • CAS No.:341973-07-7
  • Molecular Formula:C7H15NO3*ClH
  • Molecular Weight:197.662
  • Hs Code.:
(3S)-3-amino-2-hydroxy-5-methylhexanoic acid;hydrochloride

Synonyms:SCHEMBL737245

Suppliers and Price of (3S)-3-amino-2-hydroxy-5-methylhexanoic acid;hydrochloride
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (3S)-3-amino-2-hydroxy-5-methylhexanoic acid;hydrochloride
Chemical Property:
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:197.0818711
  • Heavy Atom Count:12
  • Complexity:136
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C)CC(C(C(=O)O)O)N.Cl
  • Isomeric SMILES:CC(C)C[C@@H](C(C(=O)O)O)N.Cl
Technology Process of (3S)-3-amino-2-hydroxy-5-methylhexanoic acid;hydrochloride

There total 3 articles about (3S)-3-amino-2-hydroxy-5-methylhexanoic acid;hydrochloride 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: Py*SO3, triethylamine / dimethylsulfoxide; benzene / 0.33 h / 20 - 25 °C
2: 1.) 1N HCl, 2.) 23percent HCl / 1.) 0 deg C, 18 h, 2.) 80 deg C, 11 h
With hydrogenchloride; sulfur trioxide pyridine complex; triethylamine; In dimethyl sulfoxide; benzene;
DOI:10.1021/jm00172a005
Guidance literature:
With hydrogenchloride; Multistep reaction; 1.) 0 deg C, 18 h, 2.) 80 deg C, 11 h;
DOI:10.1021/jm00172a005
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