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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,N-bis(phenylmethyl)-

OC(=O)CN(Cc1ccccc1)Cc1ccccc1 Request for Quotation
Chemical Name: Glycine, N,N-bis(phenylmethyl)-
CAS Number: 17360-47-3
Product Number: AG001Z35(AGN-PC-0JPT9Z)
Synonyms:
MDL No:
Molecular Formula: C16H17NO2
Molecular Weight: 255.3117

Identification/Properties

Properties
BP:
395.5°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
255.317g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
255.126g/mol
Monoisotopic Mass:
255.126g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
248
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

PNMR/2-DIBENZYLAMIN-17360-47-3-hnmr.pdf

Other Analytical Data

POTHER/2-DIBENZYLAMIN-17360-47-3-hplc.pdf

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Chemical Structure


2-(Dibenzylamino)acetic acid is a versatile compound widely used in chemical synthesis, particularly in the field of organic chemistry. This compound serves as a valuable building block for the synthesis of various organic molecules due to its unique structural properties and reactivity. In chemical synthesis, 2-(Dibenzylamino)acetic acid can be utilized as a key intermediate in the preparation of pharmaceutical agents, agrochemicals, and functional materials. Its functional groups and reactivity allow for the introduction of different substituents, enabling the creation of diverse molecular structures. Furthermore, the presence of the dibenzylamino group provides the potential for selective reactions, leading to the formation of specific products with desired properties. Overall, the application of 2-(Dibenzylamino)acetic acid in chemical synthesis offers a pathway for the efficient and systematic design of complex organic compounds with tailored functionalities.