CAS 1155-62-0 | L-Glutamic acid, N-[(phenylmethoxy)carbonyl]- | CAS Number 1155-62-0

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1155-62-0 | L-Glutamic acid, N-[(phenylmethoxy)carbonyl]-

CAS No: 1155-62-0 Catalog No: AG000G3D MDL No:MFCD00002801

Product Description

Catalog Number:

AG000G3D

Chemical Name:

L-Glutamic acid, N-[(phenylmethoxy)carbonyl]-

CAS Number:

1155-62-0

Molecular Formula:

C13H15NO6

Molecular Weight:

281.2613

MDL Number:

MFCD00002801

IUPAC Name:

(2S)-2-(phenylmethoxycarbonylamino)pentanedioic acid

InChI:

InChI=1S/C13H15NO6/c15-11(16)7-6-10(12(17)18)14-13(19)20-8-9-4-2-1-3-5-9/h1-5,10H,6-8H2,(H,14,19)(H,15,16)(H,17,18)/t10-/m0/s1

InChI Key:

PVFCXMDXBIEMQG-JTQLQIEISA-N

SMILES:

O=C(N[C@H](C(=O)O)CCC(=O)O)OCc1ccccc1

EC Number:

214-584-1

Properties

Complexity:

351

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

281.09g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

281.264g/mol

Monoisotopic Mass:

281.09g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

113A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

0.9

Literature

Title	Journal
An enantioselective imprinted receptor for Z-glutamate exhibiting a binding induced color change.	Chemical communications (Cambridge, England) 20041021
Synthesis and anticonvulsant evaluations of N-cbz-alpha-amino-N-alkoxyglutarimides.	Archives of pharmacal research 20040201
A substructure approach toward polymeric receptors targeting dihydrofolate reductase inhibitors. 2. Molecularly imprinted polymers against Z-l-glutamic acid showing affinity for larger molecules.	The Journal of organic chemistry 20031114