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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)-

1-Naphthalenecarbonitrile, 2-(bromomethyl)-

N#Cc1c(CBr)ccc2c1cccc2 Request for Quotation
Chemical Name: 1-Naphthalenecarbonitrile, 2-(bromomethyl)-
CAS Number: 67266-37-9
Product Number: AG01EC5J(AGN-PC-0JO443)
Synonyms:
MDL No:
Molecular Formula: C12H8BrN
Molecular Weight: 246.10262

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Bromomethyl)-1-naphthonitrile, a versatile compound used in chemical synthesis, plays a crucial role in various organic reactions. This compound serves as a valuable building block for the synthesis of a wide range of organic molecules with diverse applications in the field of medicinal chemistry, materials science, and agrochemicals. Its unique structural features make it an important intermediate in the preparation of pharmaceutical compounds, organic dyes, and fluorescent materials. Additionally, 2-(Bromomethyl)-1-naphthonitrile enables the introduction of functional groups onto aromatic systems, allowing for the creation of novel molecular architectures with tailor-made properties. Its use in chemical synthesis facilitates the development of innovative solutions for challenging synthetic transformations, making it an indispensable tool for synthetic chemists striving to expand the frontiers of organic chemistry.