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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)-

Propanoic acid, 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-,(2R)-

O=C(OCC1c2ccccc2c2c1cccc2)NC[C@H](C(=O)O)C Request for Quotation
Chemical Name: Propanoic acid, 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-,(2R)-
CAS Number: 211682-15-4
Product Number: AG003C9E(AGN-PC-0QXPG6)
Synonyms:
MDL No:
Molecular Formula: C19H19NO4
Molecular Weight: 325.3585

Identification/Properties

Properties
BP:
555.3°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
325.364g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
325.131g/mol
Monoisotopic Mass:
325.131g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
444
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpropanoic acid, an advanced chiral intermediate, is a crucial component in chemical synthesis with versatile applications. Its unique molecular structure allows it to serve as a key building block in the creation of complex pharmaceuticals, agrochemicals, and advanced materials. The chiral nature of this compound plays a vital role in controlling the stereochemistry of the final products, making it valuable in the production of enantiomerically pure compounds for various industries. In chemical synthesis, (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpropanoic acid is utilized as a pivotal reagent for asymmetric synthesis, enabling the creation of optically active compounds with high purity and selectivity. Its strategic use in asymmetric catalysis and stereoselective reactions has revolutionized the field of organic chemistry by offering efficient synthetic routes to valuable molecules. This compound's contribution to the advancement of modern chemical synthesis techniques underscores its significance as a strategic tool for researchers and professionals in the fields of chemistry, medicine, and materials science.