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1426068-26-9

3-(1,3,2-dioxaborolan-2-yl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1426068-26-9 Structure

  • Basic information

    1. Product Name: 3-(1,3,2-dioxaborolan-2-yl)benzamide
    2. Synonyms: 3-(1,3,2-dioxaborolan-2-yl)benzamide
    3. CAS NO:1426068-26-9
    4. Molecular Formula:
    5. Molecular Weight: 190.994
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1426068-26-9.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: 3-(1,3,2-dioxaborolan-2-yl)benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(1,3,2-dioxaborolan-2-yl)benzamide(1426068-26-9)
    11. EPA Substance Registry System: 3-(1,3,2-dioxaborolan-2-yl)benzamide(1426068-26-9)

  • 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: 1426068-26-9(Hazardous Substances Data)

1426068-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1426068-26-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,6,0,6 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1426068-26:
(9*1)+(8*4)+(7*2)+(6*6)+(5*0)+(4*6)+(3*8)+(2*2)+(1*6)=149
149 % 10 = 9
So 1426068-26-9 is a valid CAS Registry Number.

1426068-26-9Relevant articles and documents

Development of a Multigram synthesis of URB937, a peripherally restricted FAAH inhibitor

Fiorelli, Claudio,Scarpelli, Rita,Piomelli, Daniele,Bandiera, Tiziano

supporting information, p. 359 - 367 (2013/06/05)

A new synthetic approach to URB937 was developed starting from the inexpensive and widely available 4-benzyloxyphenol. A reproducible four-step procedure, requiring no chromatographic purifications, was optimized that allowed the preparation of 100 g of URB937 in 45% overall yield.

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