(R)-3-(1-(tert-Butoxycarbonyl)-1H-imidazol-4-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid

Base Information

• Chemical Name: (R)-3-(1-(tert-Butoxycarbonyl)-1H-imidazol-4-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid
• CAS No.: 75498-93-0
• Molecular Formula: C₁₆H₂₅N₃O₆
• Molecular Weight: 355.391
• European Community (EC) Number: 688-126-8
• Wikidata: Q76393727
• Mol file: 75498-93-0.mol

Synonyms:75498-93-0;BOC-D-HIS(BOC)-OH;(R)-3-(1-(tert-Butoxycarbonyl)-1H-imidazol-4-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid;N,1-Bis-Boc-D-histidine;(2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-[1-[(2-methylpropan-2-yl)oxycarbonyl]imidazol-4-yl]propanoic acid;SCHEMBL13650201;MFCD00270720;FD21736;AS-49189;CS-0362403;N,1-Bis[(1,1-dimethylethoxy)carbonyl]-D-histidine;(R)-3-(1-(tert-Butoxycarbonyl)-1H-imidazol-4-yl)-2-((tert-butoxycarbonyl)amino)propanoicacid

Chemical Property of (R)-3-(1-(tert-Butoxycarbonyl)-1H-imidazol-4-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid

Chemical Property:

• PSA: 119.75000
• LogP: 2.57760
• Storage Temp.: 2-8°C
• XLogP3: 1.9
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 8
• Exact Mass: 355.17433553
• Heavy Atom Count: 25
• Complexity: 509

Purity/Quality:

98% ^*data from raw suppliers

(R)-3-(1-(tert-Butoxycarbonyl)-1H-imidazol-4-yl)-2-((tert-butoxycarbonyl)amino)propanoicacid 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)OC(=O)NC(CC1=CN(C=N1)C(=O)OC(C)(C)C)C(=O)O
• Isomeric SMILES: CC(C)(C)OC(=O)N[C@H](CC1=CN(C=N1)C(=O)OC(C)(C)C)C(=O)O

Technology Process of (R)-3-(1-(tert-Butoxycarbonyl)-1H-imidazol-4-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid

There total 1 articles about (R)-3-(1-(tert-Butoxycarbonyl)-1H-imidazol-4-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid 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:

→ (Boc)-His(Boc)-OH (20866-46-0,75498-93-0)

Guidance literature:

Histidin. Di-tert-butylpyrocarbonat;

DOI:10.1007/BF00563997

Reference yield:

1-[2-(3-amino-propoxy)-5-chloro-phenyl]-3-(5-cyano-pyridin-2-yl)-urea (631863-83-7) + (Boc)-His(Boc)-OH (20866-46-0,75498-93-0) → C32H39ClN8O7

Guidance literature:

(Boc)-His(Boc)-OH; With triethylamine; HATU; In dichloromethane; at 20 ℃; for 0.0833333h;

1-[2-(3-amino-propoxy)-5-chloro-phenyl]-3-(5-cyano-pyridin-2-yl)-urea; In dichloromethane; at 20 ℃; for 1h;