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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)-

tert-butyl 4-nitropiperidine-1-carboxylate

O=C(N1CCC(CC1)[N+](=O)[O-])OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 4-nitropiperidine-1-carboxylate
CAS Number: 1228630-89-4
Product Number: AG000JMY(AGN-PC-07YLFK)
Synonyms:
MDL No:
Molecular Formula: C10H18N2O4
Molecular Weight: 230.2609

Identification/Properties

Computed Properties
Molecular Weight:
230.264g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
230.127g/mol
Monoisotopic Mass:
230.127g/mol
Topological Polar Surface Area:
75.4A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
272
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


Tert-butyl 4-nitropiperidine-1-carboxylate is a versatile chemical compound widely used in organic synthesis processes. Its application in chemical synthesis is particularly significant in the field of pharmaceuticals and agrochemicals. This compound serves as a crucial building block in the creation of various biologically active molecules and complex organic structures.One of the key uses of Tert-butyl 4-nitropiperidine-1-carboxylate is in the development of novel pharmaceuticals due to its ability to introduce specific functional groups and stereochemical elements into target molecules. Its unique structure and reactivity make it a valuable tool for chemists striving to design and synthesize new drugs with enhanced therapeutic properties. Additionally, this compound plays a pivotal role in the creation of advanced materials and fine chemicals with tailored characteristics and applications.Furthermore, Tert-butyl 4-nitropiperidine-1-carboxylate contributes to the expansion of chemical diversity and complexity in the realm of organic synthesis. By serving as a key intermediate in multi-step synthetic pathways, it enables chemists to access a wide range of structurally diverse compounds with varying properties and functionalities. This versatile compound thus facilitates the exploration of new chemical spaces and the discovery of innovative solutions in the fields of medicine, agriculture, and materials science.Overall, Tert-butyl 4-nitropiperidine-1-carboxylate stands as a valuable asset in the toolkit of synthetic chemists, offering a myriad of possibilities for creating novel molecules and advancing the frontiers of chemical research and development.