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672292-01-2

Benzamide, N-[(1S,2S)-2-hydroxy-1-(hydroxymethyl)propyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 672292-01-2 Structure

  • Basic information

    1. Product Name: Benzamide, N-[(1S,2S)-2-hydroxy-1-(hydroxymethyl)propyl]-
    2. Synonyms:
    3. CAS NO:672292-01-2
    4. Molecular Formula: C11H15NO3
    5. Molecular Weight: 209.245
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 672292-01-2.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: Benzamide, N-[(1S,2S)-2-hydroxy-1-(hydroxymethyl)propyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzamide, N-[(1S,2S)-2-hydroxy-1-(hydroxymethyl)propyl]-(672292-01-2)
    11. EPA Substance Registry System: Benzamide, N-[(1S,2S)-2-hydroxy-1-(hydroxymethyl)propyl]-(672292-01-2)

  • 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: 672292-01-2(Hazardous Substances Data)

672292-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 672292-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,2,2,9 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 672292-01:
(8*6)+(7*7)+(6*2)+(5*2)+(4*9)+(3*2)+(2*0)+(1*1)=162
162 % 10 = 2
So 672292-01-2 is a valid CAS Registry Number.

672292-01-2Relevant articles and documents

Solid-Phase Synthesis and Screening of Macrocyclic Nucleotide-Hybrid Compounds Targeted to Hepatitis C NS5B

Smietana, Michael,Johnson, Robert B.,Wang, Q. May,Kool, Eric T.

, p. 173 - 181 (2007/10/03)

A convergent strategy for the synthesis of cyclic nucleotide-hybrid molecules on controlled pore glass is reported. A major advantage of the approach is the lack of restrictions on the sequence and structural variation, allowing the incorporation of modif

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