Benzoic acid, 4-(aminocarbonyl)-, phenylmethyl ester

Base Information

Chemical Name:Benzoic acid, 4-(aminocarbonyl)-, phenylmethyl ester
CAS No.:101097-45-4
Molecular Formula:C15H13NO3
Molecular Weight:255.273
Hs Code.:
DSSTox Substance ID:DTXSID10466234
Nikkaji Number:J1.930.704B
Wikidata:Q82292754
Mol file:101097-45-4.mol

Synonyms:101097-45-4;Benzyl 4-carbamoylbenzoate;Benzoic acid, 4-(aminocarbonyl)-, phenylmethyl ester;SCHEMBL4852019;DTXSID10466234;AKOS034422175;Z51544162

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Benzoic acid, 4-(aminocarbonyl)-, phenylmethyl ester

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:255.08954328
Heavy Atom Count:19
Complexity:315

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC(=O)C2=CC=C(C=C2)C(=O)N

Technology Process of Benzoic acid, 4-(aminocarbonyl)-, phenylmethyl ester

There total 6 articles about Benzoic acid, 4-(aminocarbonyl)-, phenylmethyl ester 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: 95.0%

: 67852-95-3
4-benzyloxycarbonyl-benzoyl chloride

: 101097-45-4
4-benzyloxycarbonyl-benzamide

Guidance literature:: With ammonia; In tetrahydrofuran; at 0 ℃;
DOI:10.1016/j.bmc.2011.12.059

Reference yield: 85.0%

: 104367-76-2
4-Carbobenzoxyphenylaldoxime

: 101097-45-4
4-benzyloxycarbonyl-benzamide

Guidance literature:: RhCl(PPh₃)3; In toluene; at 150 ℃; for 4h;
DOI:10.1039/b305268k

Reference yield:

: 78767-55-2
benzyl 4-formylbenzoate

: 101097-45-4
4-benzyloxycarbonyl-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / H₂NOH*HCl

2: 85 percent / RhCl(PPh₃)3 / toluene / 4 h / 150 °C

With hydroxylamine hydrochloride; RhCl(PPh₃)3; In toluene;
DOI:10.1039/b305268k