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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)-

Carbamic acid, (6-methoxy-3-pyridinyl)-, 1,1-dimethylethyl ester

COc1ccc(cn1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: Carbamic acid, (6-methoxy-3-pyridinyl)-, 1,1-dimethylethyl ester
CAS Number: 183741-80-2
Product Number: AG00APT7(AGN-PC-0KKPAP)
Synonyms:
MDL No: MFCD07437873
Molecular Formula: C11H16N2O3
Molecular Weight: 224.2563

Identification/Properties

Computed Properties
Molecular Weight:
224.26g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
224.116g/mol
Monoisotopic Mass:
224.116g/mol
Topological Polar Surface Area:
60.4A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
238
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


The tert-Butyl (6-methoxypyridin-3-yl)carbamate is a versatile compound widely utilized in chemical synthesis due to its unique properties. Its application in organic chemistry involves acting as a protecting group for amines, particularly in the synthesis of peptide and protein molecules. By attaching the tert-Butyl (6-methoxypyridin-3-yl)carbamate to an amine moiety, it effectively shields the amine from unwanted reactions during various synthetic steps. This protecting group can be selectively removed under specific conditions, allowing for precise control over the synthetic process. This compound plays a crucial role in the efficient and controlled synthesis of complex organic molecules in the field of medicinal chemistry and drug development.