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112010-92-1

Benzeneacetamide, -alpha--hydroxy-2-(hydroxyphenylmethyl)-4,5-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Benzeneacetamide,-alpha--hydroxy-2-(hydroxyphenylmethyl)-4,5-dimethoxy-

    Cas No: 112010-92-1

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  • 112010-92-1 Structure

  • Basic information

    1. Product Name: Benzeneacetamide, -alpha--hydroxy-2-(hydroxyphenylmethyl)-4,5-dimethoxy-
    2. Synonyms: Benzeneacetamide, -alpha--hydroxy-2-(hydroxyphenylmethyl)-4,5-dimethoxy-
    3. CAS NO:112010-92-1
    4. Molecular Formula: C17H19NO5
    5. Molecular Weight: 317.34
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112010-92-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzeneacetamide, -alpha--hydroxy-2-(hydroxyphenylmethyl)-4,5-dimethoxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzeneacetamide, -alpha--hydroxy-2-(hydroxyphenylmethyl)-4,5-dimethoxy-(112010-92-1)
    11. EPA Substance Registry System: Benzeneacetamide, -alpha--hydroxy-2-(hydroxyphenylmethyl)-4,5-dimethoxy-(112010-92-1)

  • 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: 112010-92-1(Hazardous Substances Data)

112010-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112010-92-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,1 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112010-92:
(8*1)+(7*1)+(6*2)+(5*0)+(4*1)+(3*0)+(2*9)+(1*2)=51
51 % 10 = 1
So 112010-92-1 is a valid CAS Registry Number.

112010-92-1Upstream product

112010-92-1Downstream Products

112010-92-1Relevant articles and documents

Hydroxyiminoisoquinolin-3(2H)-ones. Part 7. Rearrangement of 4-Hydroxyimino-1,4-dihydroisoquinolin-3(2H)-ones under Wolff-Semmler-Type Reaction Conditions

Tikk, Istvan,Deak, Gyula,Sohar, Pal,Tamas, Jozsef

, p. 1101 - 1119 (2007/10/02)

The refluxing of 1-aryl-4-hydroximino-1,4-dihydroisoquinolin-3(2H)-ones (1 a-e) with Beckmann's mixture (AcOH/Ac2O/HCl) resulted in a hitherto unknown rearrangement to give 4-acetylamino-1-arylisoquinolin-3(2H)-ones (2 a-e).At 55 deg C, the 6,7-dimethoxy derivatives (1c) and (1d) yielded 3,4-dioxo-1-phenyl-1,2,3,4-tetrahydroisoquinolin-1-ol (6) and its N-methyl derivative (7), respectively.Reduction of these compounds with sodium borohydride caused cleavage of the hetero ring to give the acid amides (8) and (9).From the reactions at 95 deg C of the 6,7-dimethoxy derivative (1d) the oxazoloisoquinoline (10) was isolated.

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