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1414932-57-2

(1-benzyl-1H-tetrazol-5-yl)diphenylmethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1414932-57-2 Structure

  • Basic information

    1. Product Name: (1-benzyl-1H-tetrazol-5-yl)diphenylmethanol
    2. Synonyms: (1-benzyl-1H-tetrazol-5-yl)diphenylmethanol
    3. CAS NO:1414932-57-2
    4. Molecular Formula:
    5. Molecular Weight: 342.4
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1414932-57-2.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: (1-benzyl-1H-tetrazol-5-yl)diphenylmethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1-benzyl-1H-tetrazol-5-yl)diphenylmethanol(1414932-57-2)
    11. EPA Substance Registry System: (1-benzyl-1H-tetrazol-5-yl)diphenylmethanol(1414932-57-2)

  • 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: 1414932-57-2(Hazardous Substances Data)

1414932-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1414932-57-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,4,9,3 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1414932-57:
(9*1)+(8*4)+(7*1)+(6*4)+(5*9)+(4*3)+(3*2)+(2*5)+(1*7)=152
152 % 10 = 2
So 1414932-57-2 is a valid CAS Registry Number.

1414932-57-2Downstream Products

1414932-57-2Relevant articles and documents

Some practical methods for the application of 5-metallo-1-benzyl-1H- tetrazoles in synthesis

Wiedemann, Sean H.,Bio, Matthew M.,Brown, Liane M.,Hansen, Karl B.,Langille, Neil F.

, p. 2231 - 2236 (2012/11/13)

Nucleophilic reagents such as 5-lithiotetrazoles are synthetically powerful tools for the installation of tetrazole functional groups, but they are of limited utility due to the instability of tetrazole-derived carbanions. Herein, we report practical methods for the generation and use of new 5-metallo-1-benzyl-1H-tetrazoles (M=K, MgX, ZnX) derived from either 1-benzyl-1H-tetrazole or 1-benzyl-5-bromo-1H-tetrazole. By varying the metal counterion, the tetrazole carbanion stability was improved. Potassium- and magnesium-derived reagents underwent additions to carbonyl compounds at -30 and -20°C, respectively. The isolated yields (41-85%) from these and other reactions were comparable to those reported for 5-lithiotetrazoles at much lower temperatures (-78 to -98 °C). Georg Thieme Verlag Stuttgart ? New York.

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