CAS 305798-03-2
:6-Bromo-2-naphthaleneacetonitrile
Description:
6-Bromo-2-naphthaleneacetonitrile is an organic compound characterized by its naphthalene structure, which is a fused bicyclic aromatic hydrocarbon. The presence of a bromine atom at the 6-position of the naphthalene ring introduces a halogen substituent, enhancing its reactivity and potential applications in various chemical reactions. The acetonitrile functional group (-C≡N) attached to the 2-position of the naphthalene contributes to its polar nature, making it soluble in polar solvents. This compound is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in nucleophilic substitution reactions. Additionally, the presence of both aromatic and nitrile functionalities allows for diverse reactivity patterns, including electrophilic aromatic substitution and coupling reactions. Safety data should be consulted, as brominated compounds can pose health risks, and appropriate handling procedures should be followed in laboratory settings. Overall, 6-Bromo-2-naphthaleneacetonitrile is a valuable intermediate in synthetic organic chemistry.
Formula:C12H8BrN
InChI:InChI=1S/C12H8BrN/c13-12-4-3-10-7-9(5-6-14)1-2-11(10)8-12/h1-4,7-8H,5H2
InChI key:InChIKey=NZBZZSVXIBHSKR-UHFFFAOYSA-N
SMILES:C(C#N)C1=CC2=C(C=C1)C=C(Br)C=C2
Synonyms:- (6-Bromonaphthalen-2-yl)acetonitrile
- 2-Naphthaleneacetonitrile, 6-bromo-
- 2-(6-Bromonaphthalen-2-yl)acetonitrile
- 6-Bromo-2-naphthaleneacetonitrile
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