1. Home
  2. Glycine, N-(phenylmethyl)-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Glycine, N-(phenylmethyl)-

OC(=O)CNCc1ccccc1 Request for Quotation
Chemical Name: Glycine, N-(phenylmethyl)-
CAS Number: 17136-36-6
Product Number: AG003SRR(AGN-PC-0DAUF8)
Synonyms:
MDL No: MFCD00190772
Molecular Formula: C9H11NO2
Molecular Weight: 165.1891

Identification/Properties

Properties
MP:
232 °C (dec.);(lit.);
BP:
308.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
165.192g/mol
XLogP3:
-1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
165.079g/mol
Monoisotopic Mass:
165.079g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
142
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-(Benzylamino)acetic acid is a versatile compound that plays a crucial role in chemical synthesis. This compound is commonly used as a building block in the creation of various pharmaceuticals, agrochemicals, and materials. Its unique structure and chemical properties make it an important intermediate in the synthesis of complex organic molecules. The presence of both the benzyl and amino groups in its structure allows for diverse functionalization and modification, making it a valuable tool in the design and development of new compounds. In chemical synthesis, 2-(Benzylamino)acetic acid can be employed as a starting material for the preparation of a wide range of derivatives through various reaction pathways such as acylation, alkylation, and cyclization. Its presence in the synthesis pathway can impart specific properties or functionalities to the final product, making it an indispensable component in the creation of novel molecules with tailored properties for specific applications.