2H-Isoindole-2-butanoic acid, gamma-(aminocarbonyl)-1,3-dihydro-1,3-dioxo-, (S)-

Base Information

Chemical Name:2H-Isoindole-2-butanoic acid, gamma-(aminocarbonyl)-1,3-dihydro-1,3-dioxo-, (S)-
CAS No.:2614-08-6
Molecular Formula:C13H12N2O5
Molecular Weight:276.249
Hs Code.:
NSC Number:92156
DSSTox Substance ID:DTXSID80949024
Nikkaji Number:J2.440.234G
Wikidata:Q82926853

Synonyms:N-phthalylisoglutamine

Suppliers and Price of 2H-Isoindole-2-butanoic acid, gamma-(aminocarbonyl)-1,3-dihydro-1,3-dioxo-, (S)-

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

Total 5 raw suppliers

Chemical Property of 2H-Isoindole-2-butanoic acid, gamma-(aminocarbonyl)-1,3-dihydro-1,3-dioxo-, (S)-

Chemical Property:

Vapor Pressure:1.8E-14mmHg at 25°C
Boiling Point:583.8°Cat760mmHg
Flash Point:306.9°C
Density:1.508g/cm³
XLogP3:-0.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:276.07462149
Heavy Atom Count:20
Complexity:438

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(=O)N(C2=O)C(CCC(=O)O)C(=O)N
Isomeric SMILES:C1=CC=C2C(=C1)C(=O)N(C2=O)[C@@H](CCC(=O)O)C(=O)N

Technology Process of 2H-Isoindole-2-butanoic acid, gamma-(aminocarbonyl)-1,3-dihydro-1,3-dioxo-, (S)-

There total 4 articles about 2H-Isoindole-2-butanoic acid, gamma-(aminocarbonyl)-1,3-dihydro-1,3-dioxo-, (S)- 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:

: 85-44-9
phthalic anhydride

: 636-65-7
glutamine

: 2614-08-6,2820-40-8
(S)-4-phthalimidoglutaramic acid

Guidance literature:: With triethylamine; In toluene; at 110 ℃; Product distribution / selectivity;

Reference yield:

: 841-67-8
(S)-thalidomide

: 2614-08-6,2820-40-8
(S)-4-phthalimidoglutaramic acid

: 131-68-0,29883-18-9
α-(o-carboxybenzamido)-L-glutarimide

Guidance literature:: In aq. phosphate buffer; dimethyl sulfoxide; at 37 ℃; pH=7.4;
DOI:10.1002/chir.22683

Reference yield:

: 841-67-8
(S)-thalidomide

: 2614-08-6,2820-40-8
(S)-4-phthalimidoglutaramic acid

: 2614-06-4
(R)-thalidomide

: 131-68-0,29883-18-9
α-(o-carboxybenzamido)-L-glutarimide

: 3343-29-1,2110-19-2,174591-46-9
(S)-2-phthalimidoglutaramic acid

Guidance literature:: human serum albumin; In phosphate buffer; at 37 ℃; pH=7.40; Further Variations:; Catalysts; catalyst, buffer concentration; Kinetics;
DOI:10.1021/tx9801817