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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 (3-bromo-4-oxocyclohexyl)carbamate

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Chemical Name: tert-Butyl (3-bromo-4-oxocyclohexyl)carbamate
CAS Number: 1073632-93-5
Product Number: AG0093KK(AGN-PC-0WD2X4)
Synonyms:
MDL No: MFCD23115355
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
292.173g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
291.047g/mol
Monoisotopic Mass:
291.047g/mol
Topological Polar Surface Area:
55.4A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
285
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl (3-bromo-4-oxocyclohexyl)carbamate is a versatile compound widely used in chemical synthesis as a key building block for the creation of various pharmaceuticals, agrochemicals, and organic materials. Its unique structure and reactivity make it particularly valuable in the development of complex molecules through synthetic routes such as cross-coupling reactions, nucleophilic substitutions, and carbonyl chemistry. This compound's strategic placement of functional groups allows for precise manipulation of its chemical properties, leading to the efficient and selective formation of new carbon-carbon and carbon-heteroatom bonds. By incorporating tert-Butyl (3-bromo-4-oxocyclohexyl)carbamate into synthetic pathways, chemists can access diverse chemical space and unlock novel structures with potential biological or industrial significance.