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  2. 2-[1-(9H-fluoren-9-ylmethoxycarbonyl)piperidin-4-ylidene]acetic acid

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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-[1-(9H-fluoren-9-ylmethoxycarbonyl)piperidin-4-ylidene]acetic acid

OC(=O)C=C1CCN(CC1)C(=O)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: 2-[1-(9H-fluoren-9-ylmethoxycarbonyl)piperidin-4-ylidene]acetic acid
CAS Number: 885274-82-8
Product Number: AG0089GG(AGN-PC-0BSCCL)
Synonyms:
MDL No:
Molecular Formula: C22H21NO4
Molecular Weight: 363.4064

Identification/Properties

Computed Properties
Molecular Weight:
363.413g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
363.147g/mol
Monoisotopic Mass:
363.147g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
569
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 2-(1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidin-4-ylidene)acetic acid serves as a valuable tool in chemical synthesis. This molecule plays a crucial role in the creation of complex organic compounds through its reactivity and functional groups. Specifically, its piperidine moiety can participate in various synthetic transformations, making it an essential building block for the synthesis of pharmaceuticals, agrochemicals, and materials. Additionally, the fluorenyl group provides stability and structural diversity to the molecule, allowing for tailored modifications and enhanced properties in the final products. Overall, the application of this compound in chemical synthesis enables efficient and controlled processes for the production of diverse and intricate molecular structures.