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2-(1-hydroxycyclohexyl)butanenitrile is a chemical compound with the molecular formula C10H15NO. It is a derivative of butanenitrile, featuring a cyclohexyl group with a hydroxyl group attached to the first carbon and a nitrile group on the second carbon. 2-(1-hydroxycyclohexyl)butanenitrile is characterized by its unique structure, which combines the properties of a nitrile with a cyclohexane ring, making it potentially useful in various chemical applications, such as the synthesis of pharmaceuticals or other organic compounds. Its specific reactivity, solubility, and other physical properties would depend on its molecular structure and the presence of the hydroxyl and nitrile functional groups.

7178-93-0

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7178-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7178-93-0 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 7178-93:
(6*7)+(5*1)+(4*7)+(3*8)+(2*9)+(1*3)=120
120 % 10 = 0
So 7178-93-0 is a valid CAS Registry Number.

7178-93-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-hydroxycyclohexyl)butanenitrile

1.2 Other means of identification

Product number -
Other names α-(1-Hydroxy-cyclohexyl)-butyronitril

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7178-93-0 SDS

7178-93-0Relevant 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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