1. Home
  2. 4-Piperidinebutanoic acid, 1-[(9H-fluoren-9-ylmethoxy)carbonyl]-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

4-Piperidinebutanoic acid, 1-[(9H-fluoren-9-ylmethoxy)carbonyl]-

OC(=O)CCCC1CCN(CC1)C(=O)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: 4-Piperidinebutanoic acid, 1-[(9H-fluoren-9-ylmethoxy)carbonyl]-
CAS Number: 885274-47-5
Product Number: AG0089GQ(AGN-PC-01A9T2)
Synonyms:
MDL No:
Molecular Formula: C24H27NO4
Molecular Weight: 393.4755

Identification/Properties

Computed Properties
Molecular Weight:
393.483g/mol
XLogP3:
4.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
393.194g/mol
Monoisotopic Mass:
393.194g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
29
Formal Charge:
0
Complexity:
549
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The 4-(1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidin-4-yl)butanoic acid, known for its versatile properties, serves as a crucial component in chemical synthesis processes. This compound plays an indispensable role in the development and fabrication of various pharmaceuticals, agrochemicals, and specialty chemicals. With its unique structural characteristics, it acts as a key intermediate in the synthesis of complex organic molecules, enabling the creation of diverse chemical products with high purity and efficiency. Additionally, its functional groups facilitate selective reactions and enable precise control over the synthesis pathways, making it a valuable tool in the hands of chemists and researchers. The application of 4-(1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidin-4-yl)butanoic acid in chemical synthesis underscores its significance in advancing the frontiers of modern chemistry and driving innovation across various industries.