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CAS

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1362100-55-7

(+/-)-(furan-2-yl)(phenyl)(1H-tetrazol-5-yl)methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1362100-55-7 Structure

  • Basic information

    1. Product Name: (+/-)-(furan-2-yl)(phenyl)(1H-tetrazol-5-yl)methanol
    2. Synonyms: (+/-)-(furan-2-yl)(phenyl)(1H-tetrazol-5-yl)methanol
    3. CAS NO:1362100-55-7
    4. Molecular Formula:
    5. Molecular Weight: 242.237
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1362100-55-7.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: (+/-)-(furan-2-yl)(phenyl)(1H-tetrazol-5-yl)methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-(furan-2-yl)(phenyl)(1H-tetrazol-5-yl)methanol(1362100-55-7)
    11. EPA Substance Registry System: (+/-)-(furan-2-yl)(phenyl)(1H-tetrazol-5-yl)methanol(1362100-55-7)

  • 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: 1362100-55-7(Hazardous Substances Data)

1362100-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1362100-55-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,2,1,0 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1362100-55:
(9*1)+(8*3)+(7*6)+(6*2)+(5*1)+(4*0)+(3*0)+(2*5)+(1*5)=107
107 % 10 = 7
So 1362100-55-7 is a valid CAS Registry Number.

1362100-55-7Downstream Products

1362100-55-7Relevant articles and documents

Dehydrative fragmentation of 5-hydroxyalkyl-1 h -tetrazoles: A mild route to alkylidenecarbenes

Wardrop, Duncan J.,Komenda, John P.

supporting information; experimental part, p. 1548 - 1551 (2012/06/05)

The development of a mild, base-free method for the generation of alkylidenecarbenes is reported. Treatment of 5-hydroxyalkyl-1H-tetrazoles with carbodiimides generates products arising from the 1,2-rearrangement or [1,5]-C-H bond insertion of a putative alkylidenecarbene. Formation of this divalent intermediate is proposed to occur by way of a tetraazafulvene, which undergoes extrusion of 2 mol of dinitrogen. Details of this methodology, its application to the synthesis of combretastatin A-4, and an improved route to 5-hydroxyalkyl-1H-tetrazoles are described.

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