CAS 874-89-5
:4-Cyanobenzyl alcohol
Description:
4-Cyanobenzyl alcohol, with the CAS number 874-89-5, is an organic compound characterized by the presence of both a cyanide group and a hydroxyl group attached to a benzyl structure. This compound features a benzene ring substituted with a cyanomethyl group at the para position relative to the hydroxyl group. It is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity. The presence of the hydroxyl group imparts alcohol-like properties, making it soluble in polar solvents such as water and alcohols, while the cyanide group contributes to its reactivity and potential applications in organic synthesis. 4-Cyanobenzyl alcohol can be used as an intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its chemical properties include the ability to participate in nucleophilic reactions and hydrogen bonding, which can influence its behavior in various chemical environments. Safety precautions should be taken when handling this compound due to the toxicity associated with cyanide derivatives.
Formula:C8H7NO
InChI:InChI=1/C8H7NO/c9-5-7-1-3-8(6-10)4-2-7/h1-4,10H,6H2
SMILES:c1cc(ccc1C#N)CO
Synonyms:- 4-(Hydroxymethyl)benzonitrile
- Benzonitrile, 4-(Hydroxymethyl)-
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Found 5 products.
4-Cyanobenzyl alcohol, 97%
CAS:<p>4-Cyanobenzyl alcohol is used as pharmaceutical intermediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference h</p>Formula:C8H7NOPurity:97%Molecular weight:133.154-(Hydroxymethyl)benzonitrile
CAS:Formula:C8H7NOPurity:97%Color and Shape:SolidMolecular weight:133.14734-(Hydroxymethyl)benzonitrile
CAS:<p>4-(Hydroxymethyl)benzonitrile</p>Formula:C8H7NOPurity:98%Color and Shape: white to light yellow solidMolecular weight:133.15g/mol4-Cyanobenzyl alcohol
CAS:<p>4-Cyanobenzyl alcohol is a phosphane that reacts with amines to form imines. This reaction can be used as a tool for the identification of amines in protein samples. The reaction time for this reaction is about 3 hours and can only be done at room temperature. 4-Cyanobenzyl alcohol also has potent inhibition activity against cyclopentadienyl, which is an important intermediate of organic synthesis. The ruthenium complex catalyzes this reaction and it can be used as a homogeneous catalyst.</p>Formula:C8H7NOPurity:Min. 95%Color and Shape:PowderMolecular weight:133.15 g/mol




