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CAS

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86886-42-2

N-(1-hydroxy-3-(4-methoxyphenyl)propan-2-yl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 86886-42-2 Structure

  • Basic information

    1. Product Name: N-(1-hydroxy-3-(4-methoxyphenyl)propan-2-yl)acetamide
    2. Synonyms: N-(1-hydroxy-3-(4-methoxyphenyl)propan-2-yl)acetamide
    3. CAS NO:86886-42-2
    4. Molecular Formula:
    5. Molecular Weight: 223.272
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 86886-42-2.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: N-(1-hydroxy-3-(4-methoxyphenyl)propan-2-yl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(1-hydroxy-3-(4-methoxyphenyl)propan-2-yl)acetamide(86886-42-2)
    11. EPA Substance Registry System: N-(1-hydroxy-3-(4-methoxyphenyl)propan-2-yl)acetamide(86886-42-2)

  • 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: 86886-42-2(Hazardous Substances Data)

86886-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86886-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,8 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86886-42:
(7*8)+(6*6)+(5*8)+(4*8)+(3*6)+(2*4)+(1*2)=192
192 % 10 = 2
So 86886-42-2 is a valid CAS Registry Number.

86886-42-2Relevant articles and documents

Sequential Acylation/Silylation/Hetero-Claisen Rearrangement of Nitroalkanes for the Synthesis of Protected Hydroxyoxime Derivatives

Antonova, Yulia A.,Ioffe, Sema L.,Sukhorukov, Alexey Yu.,Tabolin, Andrey A.

, p. 3197 - 3213 (2021)

Sequential acylation-silylation of nitroalkanes leads to O-silylated α-acyloxyoximes in high yields. The first step of the reaction involves deprotonation of nitro compound with sodium hydride promoted by DBU or alcohol/15-crown-5 system followed by treat

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