2-(3-Oxo-2-phenylisoindolin-1-yl)acetic acid

Base Information

Chemical Name:2-(3-Oxo-2-phenylisoindolin-1-yl)acetic acid
CAS No.:88460-51-9
Molecular Formula:C16H13NO3
Molecular Weight:267.27900
Hs Code.:2933998090
DSSTox Substance ID:DTXSID20564336
Mol file:88460-51-9.mol

Synonyms:88460-51-9;2-(3-Oxo-2-phenylisoindolin-1-yl)acetic acid;2-(3-oxo-2-phenyl-1H-isoindol-1-yl)acetic acid;2-(3-Oxo-2-phenylisoindolin-1-yl)aceticacid;1H-Isoindole-1-acetic acid, 2,3-dihydro-3-oxo-2-phenyl-;SCHEMBL10551047;DTXSID20564336;IAMAZOQKJCFDLZ-UHFFFAOYSA-N;AKOS025148668;SB64216;3-oxo-2-phenylisoindoline-1-acetic acid;O10285;(3-Oxo-2-phenyl-2,3-dihydro-1H-isoindol-1-yl)acetic acid

Suppliers and Price of 2-(3-Oxo-2-phenylisoindolin-1-yl)acetic 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

Crysdot
2-(3-Oxo-2-phenylisoindolin-1-yl)aceticacid 95+%
5g
$ 897.00

Chemenu
2-(3-Oxo-2-phenylisoindolin-1-yl)aceticacid 95%
5g
$ 839.00

Alichem
2-(3-Oxo-2-phenylisoindolin-1-yl)aceticacid
5g
$ 786.98

Total 7 raw suppliers

Chemical Property of 2-(3-Oxo-2-phenylisoindolin-1-yl)acetic acid

Chemical Property:

PSA：57.61000
LogP:2.92780
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:267.08954328
Heavy Atom Count:20
Complexity:389

Purity/Quality:

98% ^*data from raw suppliers

2-(3-Oxo-2-phenylisoindolin-1-yl)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)N2C(C3=CC=CC=C3C2=O)CC(=O)O

Technology Process of 2-(3-Oxo-2-phenylisoindolin-1-yl)acetic acid

There total 3 articles about 2-(3-Oxo-2-phenylisoindolin-1-yl)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:

: 520-03-6
N-phenylphthalimide

: 88460-51-9
2,3-Dihydro-3-oxo-2-phenyl-1H-isoindole-1-acetic Acid

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / NaBH₄ / methanol; tetrahydrofuran / 2 h / 0 - 5 °C

2: toluene / 1 h / Heating

3: K₂CO₃ / methanol; H₂O / 2 h / Heating

With sodium tetrahydroborate; potassium carbonate; In tetrahydrofuran; methanol; water; toluene;
DOI:10.1248/cpb.38.3024

Reference yield:

: 18167-15-2
3-hydroxy-2-phenylisoindolin-1-one

: 88460-51-9
2,3-Dihydro-3-oxo-2-phenyl-1H-isoindole-1-acetic Acid

Guidance literature:: Multi-step reaction with 2 steps

1: toluene / 1 h / Heating

2: K₂CO₃ / methanol; H₂O / 2 h / Heating

With potassium carbonate; In methanol; water; toluene;
DOI:10.1248/cpb.38.3024