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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)-

b-Alanine,N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methoxy-

CON(C(=O)OCC1c2ccccc2c2c1cccc2)CCC(=O)O Request for Quotation
Chemical Name: b-Alanine,N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methoxy-
CAS Number: 247021-90-5
Product Number: AG002P3A(AGN-PC-0R0GSI)
Synonyms:
MDL No:
Molecular Formula: C19H19NO5
Molecular Weight: 341.3579

Identification/Properties

Properties
BP:
541.979°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
341.363g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
7
Exact Mass:
341.126g/mol
Monoisotopic Mass:
341.126g/mol
Topological Polar Surface Area:
76.1A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
460
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Utilizing 3-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methoxy)amino)propanoic acid in chemical synthesis offers a versatile tool for the modification and functionalization of organic molecules. Its strategic placement of functional groups allows for precise control over the chemical reactions it partakes in. This compound acts as a key building block in the creation of advanced materials, pharmaceuticals, and agrochemicals. Its unique structure enables it to serve as a linker or a protecting group, facilitating the synthesis of complex molecular architectures. By employing 3-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methoxy)amino)propanoic acid in chemical transformations, chemists are able to access a wide array of novel compounds with tailored properties and applications.