CAS 51605-97-1
:4-Amino-2-bromocumene
Description:
4-Amino-2-bromocumene, with the CAS number 51605-97-1, is an organic compound that belongs to the class of aromatic amines. It features a bromine atom and an amino group attached to a cumene structure, which is a derivative of isopropylbenzene. The presence of the amino group (-NH2) makes it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. This compound is typically characterized by its solid state at room temperature and may exhibit moderate solubility in organic solvents. Its reactivity is influenced by the electron-donating nature of the amino group and the electron-withdrawing effect of the bromine atom. 4-Amino-2-bromocumene can be utilized in the synthesis of dyes, pharmaceuticals, and agrochemicals, making it of interest in both industrial and research applications. Safety precautions should be observed when handling this compound, as it may pose health risks typical of aromatic amines, including potential carcinogenicity.
Formula:C9H12BrN
InChI:InChI=1/C9H12BrN/c1-6(2)7-3-4-9(11)8(10)5-7/h3-6H,11H2,1-2H3
SMILES:CC(C)c1ccc(c(c1)Br)N
Synonyms:- 2-Bromo-4-isopropylaniline
- 2-Bromo-4-(Propan-2-Yl)Aniline
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Found 6 products.
2-Bromo-4-isopropylaniline
CAS:Formula:C9H12BrNPurity:>98.0%(GC)Color and Shape:Colorless to Yellow clear liquidMolecular weight:214.112-Bromo-4-isopropylaniline
CAS:Formula:C9H12BrNPurity:96%Color and Shape:LiquidMolecular weight:214.10232-Bromo-4-isopropylaniline
CAS:<p>2-Bromo-4-isopropylaniline</p>Purity:97%Color and Shape:Colourless LiquidMolecular weight:214.10g/mol2-Bromo-4-isopropylaniline
CAS:Controlled Product<p>Applications 2-Bromo-4-isopropylaniline, is a versatile building block used in various chemical synthesis.<br></p>Formula:C9H12BrNColor and Shape:NeatMolecular weight:214.12-Bromo-4-isopropylaniline
CAS:Formula:C9H12BrNPurity:96%Color and Shape:Liquid, ClearMolecular weight:214.1062-Bromo-4-isopropylaniline
CAS:<p>2-Bromo-4-isopropylaniline is a spiroindoline that was synthesized by modification of the natural product, bryostatin. The compound has shown experimental activity against encephalomyelitis in mice. However, the mechanism of action is not known. 2-Bromo-4-isopropylaniline has been found to be an activator for ethylene and can catalyze reactions involving diphosphines and ligands. It binds to phenyl substituents on the molecule and forms x-ray crystallographic structures with high resolution. Optimization of the structure may lead to more potent analogs.</p>Formula:C9H12BrNPurity:Min. 95%Molecular weight:214.11 g/mol





