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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 (1-(6-bromopyridin-2-yl)cyclobutyl)carbamate

O=C(NC1(CCC1)c1cccc(n1)Br)OC(C)(C)C Request for Quotation
Chemical Name: tert-Butyl (1-(6-bromopyridin-2-yl)cyclobutyl)carbamate
CAS Number: 1841081-49-9
Product Number: AG00I1GB(AGN-PC-0WAMCX)
Synonyms:
MDL No:
Molecular Formula: C14H19BrN2O2
Molecular Weight: 327.2169

Identification/Properties

Computed Properties
Molecular Weight:
327.222g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
326.063g/mol
Monoisotopic Mass:
326.063g/mol
Topological Polar Surface Area:
51.2A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
337
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tert-Butyl (1-(6-bromopyridin-2-yl)cyclobutyl)carbamate is a valuable reagent commonly used in chemical synthesis for its versatile applications. This compound serves as a key building block in the creation of complex organic molecules due to its unique structural properties and reactivity. Specifically, it is widely utilized in the synthesis of pharmaceutical compounds, agrochemicals, and materials science due to its ability to introduce the cyclobutyl and pyridinyl groups into target molecules with precision. In addition, the tert-butyl protecting group plays a crucial role in controlling the regioselectivity and reactivity of the intermediate compounds, allowing for efficient and selective transformations in the synthesis process. This compound's role in chemical synthesis is vital for the development of new and innovative molecules with diverse applications in various fields of science and technology.