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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)-

(R)-2-((tert-Butoxycarbonyl)amino)-2-(2-chlor...

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Chemical Name: (R)-2-((tert-Butoxycarbonyl)amino)-2-(2-chlor...
CAS Number: 1212602-23-7
Product Number: AG009AYF(AGN-PC-0WA2J3)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
285.724g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
285.077g/mol
Monoisotopic Mass:
285.077g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
340
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of (R)-2-((tert-butoxycarbonyl)amino)-2-(2-chlorophenyl)acetic acid in chemical synthesis lies in its role as a versatile building block for the preparation of various pharmaceutical intermediates. This compound serves as a key starting material in the synthesis of chiral molecules and complex organic molecules due to its unique structural properties. With its chirality and functional groups, (R)-2-((tert-butoxycarbonyl)amino)-2-(2-chlorophenyl)acetic acid can be selectively modified through chemoselective reactions to introduce desired functionalities or stereochemistry. This compound is particularly valuable in the synthesis of bioactive compounds, pharmaceuticals, and agrochemicals where precise control over stereochemistry is crucial for biological activity and efficacy.