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Z-His-OH

Base Information Edit
  • Chemical Name:Z-His-OH
  • CAS No.:14997-58-1
  • Molecular Formula:C14H15N3O4
  • Molecular Weight:289.291
  • Hs Code.:29332900
  • European Community (EC) Number:239-084-0
  • DSSTox Substance ID:DTXSID501280353
  • Nikkaji Number:J26.598E
  • Mol file:14997-58-1.mol
Z-His-OH

Synonyms:14997-58-1;Z-His-OH;N-Cbz-L-histidine;L-Histidine, N-[(phenylmethoxy)carbonyl]-;CBZ-histidine;Nalpha-Cbz-L-histidine;Nalpha-Carbobenzoxy-L-histidine;Cbz-His-OH;(2S)-3-(1H-imidazol-5-yl)-2-(phenylmethoxycarbonylamino)propanoic acid;N-(alpha)-Carbobenzoxy-L-histidine;N-[(Benzyloxy)carbonyl]-L-histidine;MFCD00065960;(2S)-2-{[(benzyloxy)carbonyl]amino}-3-(1H-imidazol-4-yl)propanoic acid;(s)-2-(((benzyloxy)carbonyl)amino)-3-(1h-imidazol-5-yl)propanoic acid;N-Benzyloxycarbonyl-L-histidine;EINECS 239-084-0;Cbz-L-histidine;Cbz-His;N-alpha-benzyloxycarbonyl-L-histidine;Z-L-HISTIDINE;benzyloxycarbonyl-L-histidine;N-CBZ-L-HISTIDINE-OH;Z-His-OH, 99%;SCHEMBL254638;SCHEMBL9230979;((Benzyloxy)carbonyl)-L-histidine;DTXSID501280353;Nalpha -benzyloxycarbonyl-histidine;AMY31373;(S)-2-(BENZYLOXYCARBONYLAMINO)-3-(1H-IMIDAZOL-4-YL)PROPANOIC ACID;AKOS015909985;AKOS015924085;CS-W013996;FD21657;HY-W013280;Histidine, N-[(phenylmethoxy)carbonyl]-;N-[(Phenylmethoxy)carbonyl]-L-histidine;AC-17159;AS-49151;B0265;EN300-121289;A808989;W-108080

Suppliers and Price of Z-His-OH
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
  • Usbiological
  • N-alpha-Z-L-histidine
  • 5g
  • $ 333.00
  • TRC
  • Nα-Cbz-L-histidine
  • 5g
  • $ 150.00
  • TRC
  • Nα-Cbz-L-histidine
  • 100g
  • $ 1780.00
  • TCI Chemical
  • Nalpha-Carbobenzoxy-L-histidine >99.0%(T)
  • 1g
  • $ 51.00
  • TCI Chemical
  • Nalpha-Carbobenzoxy-L-histidine >99.0%(T)
  • 25g
  • $ 527.00
  • TCI Chemical
  • Nalpha-Carbobenzoxy-L-histidine >99.0%(T)
  • 5g
  • $ 145.00
  • Sigma-Aldrich
  • Z-His-OH 99%
  • 5g
  • $ 162.00
  • Iris Biotech GmbH
  • Z-L-His-OH
  • 25 g
  • $ 270.00
  • Iris Biotech GmbH
  • Z-L-His-OH
  • 5 g
  • $ 87.75
  • Frontier Specialty Chemicals
  • Z-His-OH 98%
  • 1g
  • $ 44.00
Total 72 raw suppliers
Chemical Property of Z-His-OH Edit
Chemical Property:
  • Appearance/Colour:White to off-white microcrystalline powder 
  • Vapor Pressure:4.56E-16mmHg at 25°C 
  • Melting Point:168 °C (dec.)(lit.) 
  • Refractive Index:-23.5 ° (C=6, 6mol/L HCl) 
  • Boiling Point:616.7 °C at 760 mmHg 
  • PKA:3.35±0.10(Predicted) 
  • Flash Point:326.8 °C 
  • PSA:104.31000 
  • Density:1.368 g/cm3 
  • LogP:1.72270 
  • Storage Temp.:−20°C 
  • Water Solubility.:almost transparency 
  • XLogP3:1.2
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:7
  • Exact Mass:289.10625597
  • Heavy Atom Count:21
  • Complexity:358
Purity/Quality:

99% *data from raw suppliers

N-alpha-Z-L-histidine *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn 
  • Hazard Codes:Xn 
  • Statements: 20/21/22-36/37/38 
  • Safety Statements: 22-24/25-36-26 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)COC(=O)NC(CC2=CN=CN2)C(=O)O
  • Isomeric SMILES:C1=CC=C(C=C1)COC(=O)N[C@@H](CC2=CN=CN2)C(=O)O
  • Uses Nα-Cbz-L-histidine is an N-Cbz-protected form of L-Histidine (H456010). L-Histidine is an essential amino acid that plays an important role in mitochondrial glutamine transport and has potential of abolishing oxidative stress caused by brain edema.L-Histidine promotes zinc uptake in human erythrocyes and also has potential as an antioxidant therapy for acute mammary inflammation in cattle.
Technology Process of Z-His-OH

There total 24 articles about Z-His-OH 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:
β‐cyclodextrin; In various solvent(s); at 20 ℃; for 0.116667h; pH=8;
DOI:10.1016/j.tetlet.2006.06.162
Guidance literature:
With trimethylsilyl cyanide; In tetrahydrofuran; at 0 ℃; for 10h;
Guidance literature:
With trimethylsilyl cyanide; In tetrahydrofuran; at 40 ℃; for 24h;
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