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20862-03-7

2-Naphthaleneacetonitrile, a-hydroxy-, also known as 2-(1-Hydroxyethyl)-1-naphthalenecarbonitrile, is a chemical compound with the molecular formula C12H9NO. It is a derivative of naphthalene and is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 2-Naphthaleneacetonitrile, a-hydroxyhas been studied for its potential use in the production of anti-inflammatory and anti-cancer drugs, as well as in the development of various organic compounds with biological activities. Due to its potential toxicity, it is important to handle and use 2-Naphthaleneacetonitrile, a-hydroxywith caution and in accordance with relevant safety guidelines.

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  • 20862-03-7 Structure

  • Basic information

    1. Product Name: 2-Naphthaleneacetonitrile, a-hydroxy-
    2. Synonyms:
    3. CAS NO:20862-03-7
    4. Molecular Formula: C12H9NO
    5. Molecular Weight: 183.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20862-03-7.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: 2-Naphthaleneacetonitrile, a-hydroxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Naphthaleneacetonitrile, a-hydroxy-(20862-03-7)
    11. EPA Substance Registry System: 2-Naphthaleneacetonitrile, a-hydroxy-(20862-03-7)

  • 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: 20862-03-7(Hazardous Substances Data)

20862-03-7 Usage

Uses

Used in Pharmaceutical Industry:
2-Naphthaleneacetonitrile, a-hydroxyis used as an intermediate in the synthesis of pharmaceuticals for its potential use in the production of anti-inflammatory and anti-cancer drugs. Its unique chemical structure allows for the development of various organic compounds with biological activities, making it a valuable component in the creation of new medications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Naphthaleneacetonitrile, a-hydroxyis utilized as an intermediate in the synthesis of agrochemicals. Its properties contribute to the development of compounds with pesticidal or herbicidal activities, helping to improve crop protection and yield.
Used in Organic Chemistry Research:
2-Naphthaleneacetonitrile, a-hydroxyis also used in organic chemistry research for the development of new organic compounds with potential biological activities. Its unique structure and reactivity make it a valuable tool for exploring novel chemical reactions and syntheses, further expanding the scope of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 20862-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,6 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20862-03:
(7*2)+(6*0)+(5*8)+(4*6)+(3*2)+(2*0)+(1*3)=87
87 % 10 = 7
So 20862-03-7 is a valid CAS Registry Number.

20862-03-7Relevant articles and documents

In situ evaluation of lipase performances through dynamic asymmetric cyanohydrin resolution

Sakulsombat, Morakot,Vongvilai, Pornrapee,Ramstroem, Olof

experimental part, p. 1112 - 1117 (2011/04/16)

A dynamic resolution process based on multiple reversible cyanohydrin formation coupled to lipase-mediated transesterification is demonstrated. The resulting process resulted in the efficient evaluation of complex lipase performances in asymmetric cyanohydrin acylate synthesis. Dynamic systems were generated and resolved in situ, and the effects of the reaction conditions could be directly monitored for the overall system. By this concept, the enzyme activity, chemo- and stereoselectivity for all involved substrates could be simultaneously evaluated.

Dibutyltin dimethoxide-catalyzed cyano transfer to aldehydes and imines

Yanagisawa, Akira,Matsumoto, Takuya,Kushihara, Naoyuki,Yoshida, Kazuhiro

experimental part, p. 2918 - 2922 (2011/01/05)

A novel reaction involving cyano transfer from benzophenone cyanohydrin to aldehydes and imines was realized by using dibutyltin dimethoxide as a catalyst. Various cyanohydrins and α-amino nitriles were obtained in moderate to high yields by this reaction. Ketimines also showed remarkable reactivity as cyano acceptors under conventional reaction conditions. This catalytic reaction was further applied to a three-component condensation reaction of aldehydes, aniline, and benzophenone cyanohydrin in the presence of Drierite. Copyright

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