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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)-

2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-(4-phenylphenyl)acetic acid

OC(=O)C(c1ccc(cc1)c1ccccc1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: 2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-(4-phenylphenyl)acetic acid
CAS Number: 369403-44-1
Product Number: AG00CQ9F(AGN-PC-0217KU)
Synonyms:
MDL No: MFCD02683167
Molecular Formula: C19H21NO4
Molecular Weight: 327.3743

Identification/Properties

Computed Properties
Molecular Weight:
327.38g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
327.147g/mol
Monoisotopic Mass:
327.147g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
429
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-([1,1'-Biphenyl]-4-yl)-2-((tert-butoxycarbonyl)amino)acetic acid, also known as $name$, serves as a versatile building block in chemical synthesis due to its unique structure and reactivity. This compound is commonly employed in the modification and functionalization of organic molecules, particularly in peptide synthesis and drug development. By utilizing $name$ as a key intermediate, chemists are able to introduce specific functionalities into target molecules, allowing for precise control over the desired chemical properties. Additionally, the tert-butoxycarbonyl (Boc) protecting group on the amino acid moiety of $name$ enables selective deprotection under mild conditions, making it a valuable tool in the synthesis of complex organic compounds.