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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-Bromo-6-tert-butylOXY-pyridine

CC(Oc1cccc(n1)Br)(C)C Request for Quotation
Chemical Name: 2-Bromo-6-tert-butylOXY-pyridine
CAS Number: 949160-14-9
Product Number: AG00IINJ(AGN-PC-05IUG0)
Synonyms:
MDL No:
Molecular Formula: C9H12BrNO
Molecular Weight: 230.1017

Identification/Properties

Computed Properties
Molecular Weight:
230.105g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
229.01g/mol
Monoisotopic Mass:
229.01g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
144
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-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-6-(tert-butoxy)pyridine is a versatile compound commonly used in chemical synthesis. Its unique structure and reactivity make it a valuable reagent in organic chemistry reactions. This compound is particularly useful in the formation of carbon-carbon and carbon-heteroatom bonds in various organic transformations. In the presence of suitable catalysts or reagents, 2-Bromo-6-(tert-butoxy)pyridine can undergo reactions such as coupling reactions, nucleophilic substitutions, and cross-coupling reactions. Additionally, its bromine and tert-butoxy functional groups can be selectively modified to introduce different chemical moieties into organic molecules, allowing for the synthesis of complex organic compounds with specific structural features. This compound's versatility and reactivity make it an essential building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals requiring precise control over chemical transformations.