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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 5-iodo-4-methoxypyridin-2-ylcarbamate

COc1cc(ncc1I)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-Butyl 5-iodo-4-methoxypyridin-2-ylcarbamate
CAS Number: 944935-37-9
Product Number: AG00H6CO(AGN-PC-04G0FY)
Synonyms:
MDL No:
Molecular Formula: C11H15IN2O3
Molecular Weight: 350.1529

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
350.156g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
350.013g/mol
Monoisotopic Mass:
350.013g/mol
Topological Polar Surface Area:
60.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
268
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl (5-iodo-4-methoxypyridin-2-yl) carbamate is a versatile compound widely used in chemical synthesis as a valuable building block. This compound plays a crucial role in organic synthesis due to its unique reactivity and functional group compatibility. One of the key applications of this compound is in the synthesis of complex organic molecules, especially in the pharmaceutical industry. The presence of the tert-butyl group provides steric hindrance, which can influence the selectivity and efficiency of various chemical reactions. The 5-iodo-4-methoxypyridin-2-yl moiety is a valuable synthetic handle that enables further functionalization through various coupling reactions, such as Suzuki-Miyaura cross-coupling and Buchwald-Hartwig amination.Additionally, the carbamate functionality serves as a protecting group for amines, allowing for selective transformations of other functional groups in the molecule. This compound can be used in the synthesis of drug candidates, agrochemicals, and other fine chemicals where precise control over the chemical transformations is crucial.In summary, tert-Butyl (5-iodo-4-methoxypyridin-2-yl) carbamate is a valuable tool in the toolbox of organic chemists, enabling the construction of complex molecules with high efficiency and selectivity in chemical synthesis processes.