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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 N-(4-bromo-2-cyanopyrrol-1-yl)carbamate

N#Cc1cc(cn1NC(=O)OC(C)(C)C)Br Request for Quotation
Chemical Name: tert-butyl N-(4-bromo-2-cyanopyrrol-1-yl)carbamate
CAS Number: 937047-04-6
Product Number: AG00IHR9(AGN-PC-0C6NPF)
Synonyms:
MDL No:
Molecular Formula: C10H12BrN3O2
Molecular Weight: 286.12518

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Chemical Structure


1,1-Dimethylethyl N-(4-bromo-2-cyano-1H-pyrrol-1-yl)carbamate is a valuable chemical reagent that finds wide application in chemical synthesis processes. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structural properties and reactivity. Specifically, it acts as a versatile intermediate in the synthesis of complex organic molecules by participating in key functional group transformations such as nucleophilic addition, substitution reactions, and cyclization reactions. Furthermore, its ability to act as a masked amine and carbamate functionality provides a strategic advantage in multistep synthetic routes, enabling the efficient construction of intricate molecular frameworks. Additionally, the presence of the cyano and bromo substituents offers synthetic chemists the opportunity to introduce further diversity and functionalization into the target molecules, enhancing the scope and versatility of chemical synthesis strategies.