2-(4-Bromophenyl)-2-oxoethyl 2-aminobenzoate

Base Information

Chemical Name:2-(4-Bromophenyl)-2-oxoethyl 2-aminobenzoate
CAS No.:130627-15-5
Molecular Formula:C₁₅H₁₂BrNO₃
Molecular Weight:334.169
Hs Code.:
DSSTox Substance ID:DTXSID301231493

Synonyms:2-(4-Bromophenyl)-2-oxoethyl 2-aminobenzoate;4'-Bromophenacyl anthranilate;DTXSID301231493;STK285396;AKOS005427296;130627-15-5;2-(4-Bromophenyl)-2-oxoethyl 2-aminobenzoate #;SR-01000508658;2-[(2-Aminobenzoyl)oxy]-1-(4-bromophenyl)ethanone;SR-01000508658-1

Suppliers and Price of 2-(4-Bromophenyl)-2-oxoethyl 2-aminobenzoate

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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 2-(4-Bromophenyl)-2-oxoethyl 2-aminobenzoate

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:333.00006
Heavy Atom Count:20
Complexity:353

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of 2-(4-Bromophenyl)-2-oxoethyl 2-aminobenzoate

There total 4 articles about 2-(4-Bromophenyl)-2-oxoethyl 2-aminobenzoate 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: 98.0%

: 118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4
anthranilic acid

: 99-73-0,132309-76-3
para-bromophenacyl bromide

: 130627-15-5
Anthranilsaeure-(4-bromphenacylester)

Guidance literature:: With potassium fluoride; In N,N-dimethyl-formamide; for 0.5h; Ambient temperature;
DOI:10.1021/ac50064a047

Reference yield: 71.0%

: 130627-06-4
2-nitro-benzoic acid-(4-bromo-phenacyl ester)

: 130627-15-5
Anthranilsaeure-(4-bromphenacylester)

Guidance literature:: With hydrogen; platinum; In ethanol; Ambient temperature;

Reference yield:

: 552-16-9,104810-18-6
ortho-nitrobenzoic acid

: 130627-15-5
Anthranilsaeure-(4-bromphenacylester)

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / Et₃N / acetone / 0.5 h / Heating

2: 71 percent / Pt, H₂ / ethanol / Ambient temperature

With hydrogen; triethylamine; platinum; In ethanol; acetone;