2,3-Diphenylpropionic acid

Base Information

Chemical Name:2,3-Diphenylpropionic acid
CAS No.:3333-15-1
Molecular Formula:C₁₅H₁₄O₂
Molecular Weight:226.275
Hs Code.:29163990
European Community (EC) Number:222-065-6
NSC Number:11135,49
DSSTox Substance ID:DTXSID801311088
Nikkaji Number:J205.420E
Mol file:3333-15-1.mol

Synonyms:2,3-diphenylpropanoic acid;2,3-Diphenylpropionic acid;3333-15-1;2,3-Diphenyl-Propionic Acid;EINECS 222-065-6;MFCD00044405;Maybridge3_003394;2,3-diphenylpropanoicacid;NSC49;2,3-diphenyl-propanoic acid;Oprea1_394675;SCHEMBL67234;NSC 49;NSC-49;DTXSID801311088;HMS1440K06;NSC11135;NSC 11135;NSC-11135;AKOS001584772;AKOS016038005;AB92818;CCG-253843;IDI1_014781;AS-47862;D1790;EU-0000158;FT-0609738;F16387;SR-01000389475;PYRIDINE-2-CARBOXALDEHYDE2-QUINOLYLHYDRAZONE;SR-01000389475-1

Suppliers and Price of 2,3-Diphenylpropionic acid

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
2,3-Diphenylpropionic Acid
50mg
$ 45.00

TRC
2,3-Diphenylpropionic Acid
100mg
$ 60.00

TCI Chemical
2,3-Diphenylpropionic Acid >98.0%(GC)(T)
25g
$ 460.00

TCI Chemical
2,3-Diphenylpropionic Acid >98.0%(GC)(T)
5g
$ 134.00

Crysdot
2,3-Diphenylpropanoicacid 95+%
1g
$ 59.00

Crysdot
2,3-Diphenylpropanoicacid 95+%
5g
$ 188.00

Crysdot
2,3-Diphenylpropanoicacid 95+%
25g
$ 594.00

Chemenu
2,3-Diphenylpropanoicacid 95%
25g
$ 561.00

Biosynth Carbosynth
2,3-Diphenylpropanoic acid
10 g
$ 609.00

Biosynth Carbosynth
2,3-Diphenylpropanoic acid
5 g
$ 358.00

Total 38 raw suppliers

Chemical Property of 2,3-Diphenylpropionic acid

Chemical Property:

Vapor Pressure:4.86E-05mmHg at 25°C
Melting Point:89°C
Boiling Point:340 °C
PKA:4.18±0.10(Predicted)
Flash Point:238.6°C
PSA：37.30000
Density:1.161g/cm³
LogP:3.09750
XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:226.099379685
Heavy Atom Count:17
Complexity:237

Purity/Quality:

99%, ^*data from raw suppliers

2,3-Diphenylpropionic Acid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 36/37/38
Safety Statements: 26-36/37/39

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 2,3-Diphenylpropionic acid

There total 29 articles about 2,3-Diphenylpropionic 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: 96.0%

: C₂₁H₃₀O₂Si₂

: 3333-15-1,17040-62-9,19041-32-8,94942-89-9
(2S)-2,3-diphenylpropanoic acid

Guidance literature:: With methanol; 2,6-bis(1,3-dimethylphenanthren-9-yl)-4H-dinaphtho[2,1-d:1',2'-f][1,3,2]dithiazepine 3,3,5,5-tetraoxide; In dichloromethane; at 20 ℃; for 0.25h; enantioselective reaction; Inert atmosphere;
DOI:10.1002/anie.201905623

Reference yield: 85.0%

: 103-82-2
phenylacetic acid

: 100-39-0
benzyl bromide

: 3333-15-1,17040-62-9,19041-32-8,94942-89-9
(2S)-2,3-diphenylpropanoic acid

Guidance literature:: phenylacetic acid; With n-butyllithium; N¹,N³-bis((R)-1-phenyl-2-(piperidin-1-yl)ethyl)propane-1,3-diamine; In tetrahydrofuran; hexanes; at 0 ℃; Inert atmosphere;

benzyl bromide; In tetrahydrofuran; hexanes; at -78 ℃; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/ja205107x

Reference yield: 26.0%

: (E)-(4-(4-(trifluoromethyl)phenyl)but-3-ene-1,2-diyl)dibenzene

: 3333-15-1,17040-62-9,19041-32-8,94942-89-9
(2S)-2,3-diphenylpropanoic acid

Guidance literature:: With tetrachloromethane; sodium periodate; ruthenium(III) trichloride hydrate; water; In acetonitrile; at 20 ℃; for 2h;
DOI:10.1021/ol502279u