2-(1-((Benzyloxy)carbonyl)hydrazinyl)acetic acid

Base Information

• Chemical Name: 2-(1-((Benzyloxy)carbonyl)hydrazinyl)acetic acid
• CAS No.: 124676-23-9
• Molecular Formula: C₁₀H₁₂N₂O₄
• Molecular Weight: 224.216
• DSSTox Substance ID: DTXSID40594094
• Wikidata: Q72440676
• Mol file: 124676-23-9.mol

Synonyms:2-(1-((Benzyloxy)carbonyl)hydrazinyl)acetic acid;124676-23-9;2-[amino(phenylmethoxycarbonyl)amino]acetic acid;DTXSID40594094;{1-[(Benzyloxy)carbonyl]hydrazinyl}acetic acid;2-(1-((Benzyloxy)carbonyl)hydrazinyl)aceticacid

Chemical Property of 2-(1-((Benzyloxy)carbonyl)hydrazinyl)acetic acid

Chemical Property:

• Melting Point: 142-144℃
• Density: 1.348
• Storage Temp.: 2-8°C
• XLogP3: -1.8
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 5
• Exact Mass: 224.07970687
• Heavy Atom Count: 16
• Complexity: 251

Purity/Quality:

98%min ^*data from raw suppliers

2-(1-((Benzyloxy)carbonyl)hydrazinyl)aceticacid 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)COC(=O)N(CC(=O)O)N

Technology Process of 2-(1-((Benzyloxy)carbonyl)hydrazinyl)acetic acid

There total 2 articles about 2-(1-((Benzyloxy)carbonyl)hydrazinyl)acetic 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: 70.0%

2-(benzotriazol-1-yl)-N-(benzyloxycarbonyl)glycine (124676-19-3) → α-(N-benzyloxycarbonyl)aminoglycine (124676-23-9)

Guidance literature:

With ammonia; In methanol; at 25 ℃; for 24h;

DOI:10.1021/jo00294a042

Reference yield:

O-benzyl carbamate (621-84-1) → α-(N-benzyloxycarbonyl)aminoglycine (124676-23-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 78 percent / p-toluenesulphonic acid / benzene

2: 70 percent / NH₃ / methanol

With ammonia; toluene-4-sulfonic acid; In methanol; benzene;

DOI:10.1039/c39890000337

Reference yield: 85.0%

α-(N-benzyloxycarbonyl)aminoglycine (124676-23-9) + 1-Benzyl-5-nitro-1H-imidazole-4-carboxylic acid pentafluorophenyl ester (204527-99-1) → [(1-Benzyl-5-nitro-1H-imidazole-4-carbonyl)-amino]-benzyloxycarbonylamino-acetic acid (210036-01-4)

Guidance literature:

With triethylamine; In N,N-dimethyl-formamide; for 2h;

DOI:10.1080/07328319808004227

upstream raw materials:

2-(benzotriazol-1-yl)-N-(benzyloxycarbonyl)glycine

O-benzyl carbamate

Downstream raw materials:

1-(N-Fluorenylmethyloxycarbonyl-L-alanylamino)-1-((benzyloxycarbonyl)amino)acetic acid

[(1-Benzyl-5-nitro-1H-imidazole-4-carbonyl)-amino]-benzyloxycarbonylamino-acetic acid

[(5-Amino-1-benzyl-1H-imidazole-4-carbonyl)-amino]-benzyloxycarbonylamino-acetic acid methyl ester

[(1-Benzyl-5-nitro-1H-imidazole-4-carbonyl)-amino]-benzyloxycarbonylamino-acetic acid methyl ester

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