(4R)-5-amino-4-(1,3-dioxoisoindol-2-yl)-5-oxopentanoic acid

Base Information

Chemical Name:(4R)-5-amino-4-(1,3-dioxoisoindol-2-yl)-5-oxopentanoic acid
CAS No.:2614-09-7
Molecular Formula:C₁₃H₁₂N₂O₅
Molecular Weight:276.249
Hs Code.:
NSC Number:92155
Nikkaji Number:J3.498.187F
Mol file:2614-09-7.mol

Synonyms:2614-09-7;(4R)-5-amino-4-(1,3-dioxoisoindol-2-yl)-5-oxopentanoic acid;NSC92155;NSC-92155

Suppliers and Price of (4R)-5-amino-4-(1,3-dioxoisoindol-2-yl)-5-oxopentanoic 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
D-4-Phthalimido-glutaramicAcid
100mg
$ 1320.00

Total 2 raw suppliers

Chemical Property of (4R)-5-amino-4-(1,3-dioxoisoindol-2-yl)-5-oxopentanoic acid

Chemical Property:

Vapor Pressure:1.8E-14mmHg at 25°C
Boiling Point:583.8°Cat760mmHg
Flash Point:306.9°C
PSA：117.77000
Density:1.508g/cm³
LogP:0.63950
Solubility.:Dimethylformamide, Dimethyl Sulfoxide,
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

D-4-Phthalimido-glutaramicAcid ^*data from reagent 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
Uses Thalidomide (T338850) derivative.

Technology Process of (4R)-5-amino-4-(1,3-dioxoisoindol-2-yl)-5-oxopentanoic acid

There total 2 articles about (4R)-5-amino-4-(1,3-dioxoisoindol-2-yl)-5-oxopentanoic 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:

: 2614-06-4
(R)-thalidomide

: 2614-09-7,2820-40-8
(R)-4-phthalimidoglutaramic acid

: 841-67-8
(S)-thalidomide

: 2110-19-2,174591-46-9
(R)-2-phthalimidoglutaramic acid

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

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