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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, (5-bromo-3-pyridinyl)-, 1,1-dimethylethyl ester

O=C(OC(C)(C)C)Nc1cncc(c1)Br Request for Quotation
Chemical Name: Carbamic acid, (5-bromo-3-pyridinyl)-, 1,1-dimethylethyl ester
CAS Number: 361550-43-8
Product Number: AG00I75Z(AGN-PC-008EN1)
Synonyms:
MDL No:
Molecular Formula: C10H13BrN2O2
Molecular Weight: 273.1264

Identification/Properties

Properties
MP:
143-148℃
BP:
286.5°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
273.13g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
272.016g/mol
Monoisotopic Mass:
272.016g/mol
Topological Polar Surface Area:
51.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
228
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl (5-bromopyridin-3-yl)carbamate is a versatile chemical compound commonly used in chemical synthesis processes. Due to its unique structure and properties, this compound plays a crucial role in numerous reactions and transformations in organic chemistry.One of the key applications of tert-Butyl (5-bromopyridin-3-yl)carbamate is as a protecting group for amines in organic synthesis. By selectively masking the amino group with this compound, chemists can prevent unwanted side reactions or protect the amine functionality during the course of a multi-step synthesis. This protective step allows for the manipulation of other functional groups within a molecule without affecting the amine group, providing greater control over the reaction sequence.Furthermore, tert-Butyl (5-bromopyridin-3-yl)carbamate can also serve as a valuable building block in the preparation of various heterocyclic compounds and pharmaceutical intermediates. Its presence in a molecule can facilitate the introduction of diverse functional groups and enhance the overall synthetic efficiency.Overall, the tert-Butyl (5-bromopyridin-3-yl)carbamate compound is a versatile tool in the toolbox of synthetic chemists, enabling the construction of complex molecular structures and the development of novel chemical entities.