N-Formyl-L-histidine

Base Information

• Chemical Name: N-Formyl-L-histidine
• CAS No.: 15191-21-6
• Molecular Formula: C7H9N3O3
• Molecular Weight: 183.167
• Hs Code.: 2933290090
• European Community (EC) Number: 239-248-1
• DSSTox Substance ID: DTXSID901315407
• Nikkaji Number: J208.510K
• ChEMBL ID: CHEMBL1741817
• Mol file: 15191-21-6.mol

Synonyms:N-Formyl-L-histidine;15191-21-6;(S)-2-Formamido-3-(1H-imidazol-4-yl)propanoic acid;L-Histidine, N-formyl-;(2S)-2-formamido-3-(1H-imidazol-5-yl)propanoic acid;(2S)-3-(1H-imidazol-4-yl)-2-formamidopropanoic acid;2-formamido-3-(1H-imidazol-5-yl)propanoic acid;N-Formylhistidine;formylhistidine;NSC-334340;N-Formylhistidine #;NCIStruc1_000292;NCIStruc2_000029;SCHEMBL61920;CHEMBL1741817;WFQVSLVQIFFQQN-LURJTMIESA-N;DTXSID901315407;CCG-38324;MFCD00059159;NCGC00014776;NCI334340;AKOS010366495;HY-W142169;N-Formyl-L-histidine (For-L-His-OH);NCGC00014776-02;NCGC00097877-01;AS-68426;CS-0201951;F0133;T71824;(2S)-2-(Formylamino)-3-(1H-imidazol-4-yl)propanoic acid, AldrichCPR

Chemical Property of N-Formyl-L-histidine

Chemical Property:

• Vapor Pressure: 1.72E-17mmHg at 25°C
• Melting Point: 202.0 to 206.0 °C
• Refractive Index: 58 ° (C=2, H2O)
• Boiling Point: 442.9 °C at 760 mmHg
• Flash Point: 221.6 °C
• PSA: 95.08000
• Density: 1.51 g/cm³
• LogP: 0.17820
• Storage Temp.: Sealed in dry,Room Temperature
• Water Solubility.: almost transparency
• XLogP3: -0.7
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 183.06439116
• Heavy Atom Count: 13
• Complexity: 197

Purity/Quality:

98%,99%, ^*data from raw suppliers

N-Formyl-L-histidine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(NC=N1)CC(C(=O)O)NC=O
• Isomeric SMILES: C1=C(NC=N1)C[C@@H](C(=O)O)NC=O

Technology Process of N-Formyl-L-histidine

There total 3 articles about N-Formyl-L-histidine 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:

Reference yield:

formic acid (64-18-6) + D,L-histidine (71-00-1) → Nα-formyl-histidine (15191-21-6)

Guidance literature:

Reference yield:

formic acid (64-18-6) + L-histidine (71-00-1) → Nα-formyl-histidine (15191-21-6)

Guidance literature:

Reference yield:

formic acid (64-18-6) + D,L-histidine (71-00-1) → Nα-formyl-histidine (15191-21-6)

Guidance literature:

N^α-formyl-dl-histidine;

upstream raw materials:

formic acid

D,L-histidine

L-histidine