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309279-56-9

2-Tetrazol-1-yl-benzoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 309279-56-9 Structure

  • Basic information

    1. Product Name: 2-Tetrazol-1-yl-benzoic acid methyl ester
    2. Synonyms: 2-Tetrazol-1-yl-benzoic acid methyl ester;Methyl 2-(1-Tetrazolyl)benzoate;methyl 2-(1H-tetraazol-1-yl)benzoate
    3. CAS NO:309279-56-9
    4. Molecular Formula: C9H8N4O2
    5. Molecular Weight: 204.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 309279-56-9.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: 2-Tetrazol-1-yl-benzoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Tetrazol-1-yl-benzoic acid methyl ester(309279-56-9)
    11. EPA Substance Registry System: 2-Tetrazol-1-yl-benzoic acid methyl ester(309279-56-9)

  • 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: 309279-56-9(Hazardous Substances Data)

309279-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 309279-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,9,2,7 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 309279-56:
(8*3)+(7*0)+(6*9)+(5*2)+(4*7)+(3*9)+(2*5)+(1*6)=159
159 % 10 = 9
So 309279-56-9 is a valid CAS Registry Number.

309279-56-9Downstream Products

309279-56-9Relevant articles and documents

Application of cyclic ketones in MCR: Ugi/amide coupling based synthesis of fused tetrazolo[1,5-a][1,4]benzodiazepines

Yerande, Swapnil G.,Newase, Kiran M.,Singh, Bhawani,Boltjes, André,D?mling, Alexander

supporting information, p. 3263 - 3266 (2014/06/09)

Azido-Ugi reaction involving cyclic ketone, primary amine, isonitrile, and azide afforded substituted tetrazole derivatives 5. These intermediates were hydrolyzed to corresponding acid derivatives. EDAC/HOBt mediated amide bond formation of 5 gave fused tetrazolo[1,5-a][1,4]benzodiazepine 6 in high yield and good diversity.

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