2-amino-N-(1-phenylethyl)benzamide

Base Information

Chemical Name:2-amino-N-(1-phenylethyl)benzamide
CAS No.:85592-80-9
Molecular Formula:C15H16N2O
Molecular Weight:240.305
Hs Code.:2924299090
European Community (EC) Number:852-193-3
DSSTox Substance ID:DTXSID90383899
ChEMBL ID:CHEMBL1300276
Mol file:85592-80-9.mol

Synonyms:2-amino-N-(1-phenylethyl)benzamide;85592-80-9;2-Amino-N-(1-phenyl-ethyl)-benzamide;Maybridge1_000817;Probes2_000079;Cambridge id 5108469;Oprea1_208789;CBDivE_010603;MLS000517043;SCHEMBL4278021;CHEMBL1300276;HMS543N03;DTXSID90383899;HMS2670K09;BBL008609;MFCD00115985;STK400023;AKOS000263273;AKOS016050342;AB03486;2-amino-N~1~-(1-phenylethyl)benzamide;SMR000343221;VS-01957;CS-0206257;FT-0702149;EN300-06308;AB00073867-01;AG-205/04783049;Z56040661;2,2-Dimethyl-N-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)pyridin-2-yl]propionamide

Suppliers and Price of 2-amino-N-(1-phenylethyl)benzamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
2-?Amino-?N-?(1-?phenyl-?ethyl)?-?benzamide
1g
$ 50.00

Crysdot
2-Amino-N-(1-phenylethyl)benzamide 95+%
25g
$ 527.00

Biosynth Carbosynth
2-Amino-N-(1-phenylethyl)benzamide
10 g
$ 609.00

Biosynth Carbosynth
2-Amino-N-(1-phenylethyl)benzamide
1 g
$ 105.00

Biosynth Carbosynth
2-Amino-N-(1-phenylethyl)benzamide
500 mg
$ 60.00

Biosynth Carbosynth
2-Amino-N-(1-phenylethyl)benzamide
2 g
$ 179.00

Biosynth Carbosynth
2-Amino-N-(1-phenylethyl)benzamide
5 g
$ 358.00

Aronis compounds
2-amino-N-(1-phenylethyl)benzamide
5g
$ 321.00

American Custom Chemicals Corporation
2-AMINO-N-(1-PHENYLETHYL)BENZAMIDE 95.00%
5G
$ 1082.56

American Custom Chemicals Corporation
2-AMINO-N-(1-PHENYLETHYL)BENZAMIDE 95.00%
2.5G
$ 906.27

Total 11 raw suppliers

Chemical Property of 2-amino-N-(1-phenylethyl)benzamide

Chemical Property:

PSA：55.12000
LogP:3.73190
Storage Temp.:2-8°C
Solubility.:DMSO (Slightly), Methanol (Sparingly)
XLogP3:3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:240.126263138
Heavy Atom Count:18
Complexity:274

Purity/Quality:

99.0% ^*data from raw suppliers

2-?Amino-?N-?(1-?phenyl-?ethyl)?-?benzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C1=CC=CC=C1)NC(=O)C2=CC=CC=C2N
Uses 2-?Amino-?N-?(1-?phenyl-?ethyl)?-?benzamide is a reagent used in the synthesis of potent inhibitors of class III histone/protein deacetylases. As well, used to prepare agents promoting anticonvulsant activity.

Technology Process of 2-amino-N-(1-phenylethyl)benzamide

There total 4 articles about 2-amino-N-(1-phenylethyl)benzamide 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: 85.0%

: 118-48-9
isatoic anhydride

: 618-36-0
rac-methylbenzylamine

: 85592-80-9
2-amino-N-(1-phenylethyl)benzamide

Guidance literature:: In N,N-dimethyl-formamide; at 45 - 50 ℃; for 3h;

Reference yield:

: 124264-90-0
2-nitro-N-(1-phenylethyl)benzamide

: 85592-80-9
2-amino-N-(1-phenylethyl)benzamide

Guidance literature:: With hydrogen; palladium on activated charcoal; at 20 ℃;

Reference yield:

: 118-48-9
isatoic anhydride

: 3886-69-9
(R)-1-phenyl-ethyl-amine

: 85592-80-9
2-amino-N-(1-phenylethyl)benzamide

Guidance literature:: With acidic derivative zeolite-type small pore size adsorbent Ersorb-4, E₄a; In ethanol; at 80 ℃; for 24h;
DOI:10.1080/00397911.2014.894525