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1138-80-3 | Glycine, N-[(phenylmethoxy)carbonyl]-
CAS No: 1138-80-3 Catalog No: AG0009QA MDL No:MFCD00002691
Product Description
Catalog Number:
AG0009QA
Chemical Name:
Glycine, N-[(phenylmethoxy)carbonyl]-
CAS Number:
1138-80-3
Molecular Formula:
C10H11NO4
Molecular Weight:
209.1986
MDL Number:
MFCD00002691
IUPAC Name:
2-(phenylmethoxycarbonylamino)acetic acid
InChI:
InChI=1S/C10H11NO4/c12-9(13)6-11-10(14)15-7-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,11,14)(H,12,13)
InChI Key:
CJUMAFVKTCBCJK-UHFFFAOYSA-N
SMILES:
O=C(NCC(=O)O)OCc1ccccc1
EC Number:
214-516-0
NSC Number:
2526
Properties
Complexity:
224
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
209.069g/mol
Formal Charge:
0
Heavy Atom Count:
15
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
209.201g/mol
Monoisotopic Mass:
209.069g/mol
Rotatable Bond Count:
5
Topological Polar Surface Area:
75.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1
Literature
| Title | Journal |
|---|---|
| Imidazolopiperazines: lead optimization of the second-generation antimalarial agents. | Journal of medicinal chemistry 20120510 |
| Controlled functionalization of carbon nanotubes by a solvent-free multicomponent approach. | ACS nano 20101228 |
| Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine alpha-hydroxylating monooxygenase (PHM). | Bioorganic & medicinal chemistry 20081201 |
| Duality of mechanism in the tetramethylfluoroformamidinium hexafluorophosphate-mediated synthesis of N-benzyloxycarbonylamino acid fluorides. | The Journal of organic chemistry 20010824 |
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