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2-(1-hydroxycyclohexyl)-2-methylpropanenitrile is a chemical compound with the molecular formula C10H17NO. It is a derivative of cyclohexane, featuring a hydroxyl group (-OH) attached to the cyclohexyl ring, and a nitrile group (-CN) on the 2-methylpropane side chain. 2-(1-hydroxycyclohexyl)-2-methylpropanenitrile is known for its unique structure and potential applications in various chemical and pharmaceutical industries. It is often used as an intermediate in the synthesis of other complex organic molecules, such as pharmaceuticals and agrochemicals. Due to its specific functional groups, it can participate in various chemical reactions, including nucleophilic addition, substitution, and elimination reactions. The compound's properties, such as solubility and reactivity, can be influenced by the presence of these functional groups, making it a versatile building block in organic synthesis.

7178-96-3

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7178-96-3 Usage

Type of compound

Nitrile derivative

Functional groups

Hydroxyl group, Methyl group, Cyclohexyl ring

Usage

Synthesis of pharmaceuticals and agrochemicals

Potential application

Ligand in organometallic chemistry

Importance

Important intermediate in organic synthesis

Area of interest

Chemical research

Check Digit Verification of cas no

The CAS Registry Mumber 7178-96-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,7 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7178-96:
(6*7)+(5*1)+(4*7)+(3*8)+(2*9)+(1*6)=123
123 % 10 = 3
So 7178-96-3 is a valid CAS Registry Number.

7178-96-3Relevant academic research and scientific papers

Nucleophilic addition of α-(dimethylsilyl)nitriles to aldehydes and ketones

Jinzaki, Takaaki,Arakawa, Mitsuru,Kinoshita, Hidenori,Ichikawa, Junji,Miura, Katsukiyo

supporting information, p. 3750 - 3753 (2013/08/23)

α-Alkylated (dimethylsilyl)acetonitriles (Me2HSiCR 3R4CN) react spontaneously with aldehydes in DMSO to give β-hydroxynitriles in good to high yields. The addition to ketones is effectively promoted by using MgCl2/su

Electroorganic Chemistry. 140. Electroreductively Intra- and Intermolecular Couplings of Ketones with Nitriles

Shono, Tatsuya,Kise, Naoki,Fujimoto, Taku,Tominaga, Naoto,Morita, Hiroshi

, p. 7175 - 7187 (2007/10/02)

Electroreduction of γ- and δ-cyano ketones in i-PrOH with Sn cathode gave α-hydroxy ketones and their dehydroxylated ketones as the intramolecularly coupled products.Guaiazulene, (-)-valeranone, polyquinanes, dihydrojasmone, methyl dihydrojasmonate, and rosaprostol have been synthesized by utilizing this electroreductive intramolecular coupling of γ- and δ-cyano ketones in one of the key steps.Similarly, electroreduction of a mixture of ketone and nitrile gave the corresponding intermolecularly coupled product.The product obtained by the electroreductive intermolecular coupling of (+)-dihydrocarvone with acetonitrile has been found to be the precursor of an effective chiral ligand for the enantioselective addition of diethylzinc to aldehydes.

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