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1-Hydroxy-4-methylcyclohexanecarbonitrile is a chemical compound with the molecular formula C8H13NO. It is a derivative of cyclohexane, featuring a hydroxyl group (-OH) at the 1st position, a methyl group (-CH3) at the 4th position, and a nitrile group (-CN) at the carbon chain. 1-hydroxy-4-methylcyclohexanecarbonitrile is an organic molecule that can be used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Due to its unique structure, it possesses specific chemical properties, such as reactivity towards nucleophiles and electrophiles, making it a valuable building block in organic chemistry.

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  • 933-45-9 Structure
  • Basic information

    1. Product Name: 1-hydroxy-4-methylcyclohexanecarbonitrile
    2. Synonyms: 1-hydroxy-4-methylcyclohexanecarbonitrile
    3. CAS NO:933-45-9
    4. Molecular Formula:
    5. Molecular Weight: 139.197
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 933-45-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-hydroxy-4-methylcyclohexanecarbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-hydroxy-4-methylcyclohexanecarbonitrile(933-45-9)
    11. EPA Substance Registry System: 1-hydroxy-4-methylcyclohexanecarbonitrile(933-45-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 933-45-9(Hazardous Substances Data)

933-45-9 Usage

Appearance

White solid the compound has a pale, opaque, and crystalline appearance.

Molecular weight

139.2 g/mol the mass of one mole of 1-hydroxy-4-methylcyclohexanecarbonitrile.

Uses

Intermediate in synthesis commonly used as an intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds.

Building block

Organic synthesis serves as a fundamental component in creating more complex organic molecules.

Toxicity

Potential toxic effects the compound is known to have possible harmful effects on health and should be handled with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 933-45-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 933-45:
(5*9)+(4*3)+(3*3)+(2*4)+(1*5)=79
79 % 10 = 9
So 933-45-9 is a valid CAS Registry Number.

933-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-4-methyl-cyclohexanecarbonitrile

1.2 Other means of identification

Product number -
Other names 1-Cyano-1-hydroxy-4-methylcyclohexane

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:933-45-9 SDS

933-45-9Relevant articles and documents

CYCLOALKYLNITRILE PYRAZOLE CARBOXAMIDES AS JANUS KINASE INHIBITORS

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Page/Page column 113, (2013/04/10)

Cycloalkylnitrile pyrazole carboxamides as JAK inhibitors useful for the treatment of JAK-mediated diseases such as rheumatoid arthritis, asthma, COPD and cancer are provided.

Novel 4H-1,2,4-triazol-3-yl cycloalkanols as potent antitubercular agents

Desai, Nutan H. Palsule,Bairwa, Ranjeet,Kakwani, Manoj,Tawari, Nilesh,Ray,Rajan,Degani, Mariam

, p. 401 - 408 (2013/03/13)

Enzymes of shikimate pathway, dehydroquinase and shikimate kinase represent comparatively newer targets for antitubercular research. Molecular hybridization approach was implemented by integrating the essential features of inhibitors acting on these enzymes of shikimate pathway. Considering the flexibility of alicyclic ring of reported dehydroquinase (DHQ) inhibitors and triazole ring, key feature of the virtual hits of Mtb shikimate kinase, a series of structurally novel, substituted 4H-1,2,4-triazol-3-yl cycloalkanols were designed as antimycobacterial agents. Docking studies of the molecules was carried out on the enzyme DHQ. All the synthesized compounds exhibited promising activity (MIC 0.59-15.5 μg/ml) against H37Rv strains of Mycobacterium tuberculosis using resazurin microtiter assay. Five of the evaluated compounds exhibit MIC 50 values indicate compounds are non-toxic, with selectivity indices >28. These compounds could serve as leads for further optimization to obtain novel antimycobacterial agents.

Synthetic Studies toward Verrucarol. 1. Synthesis of the AB Ring System

Kraus, George A.,Frazier, Kevin

, p. 4820 - 4825 (2007/10/02)

A synthetic route to the AB ring system of verrucarol is described.After two routes employing intramolecular cyclization failed, the Diels-Alder reaction of methyl coumalate and isoprene afforded bicyclic lactone 13.Transformation of 13 into hydroxy lacto

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