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897599-06-3

(1H-benzo[d][1,2,3]triazol-1-yl)[4-(benzyloxy)phenyl]methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 897599-06-3 Structure

  • Basic information

    1. Product Name: (1H-benzo[d][1,2,3]triazol-1-yl)[4-(benzyloxy)phenyl]methanone
    2. Synonyms: (1H-benzo[d][1,2,3]triazol-1-yl)[4-(benzyloxy)phenyl]methanone
    3. CAS NO:897599-06-3
    4. Molecular Formula:
    5. Molecular Weight: 329.358
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 897599-06-3.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: (1H-benzo[d][1,2,3]triazol-1-yl)[4-(benzyloxy)phenyl]methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1H-benzo[d][1,2,3]triazol-1-yl)[4-(benzyloxy)phenyl]methanone(897599-06-3)
    11. EPA Substance Registry System: (1H-benzo[d][1,2,3]triazol-1-yl)[4-(benzyloxy)phenyl]methanone(897599-06-3)

  • 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: 897599-06-3(Hazardous Substances Data)

897599-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 897599-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,7,5,9 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 897599-06:
(8*8)+(7*9)+(6*7)+(5*5)+(4*9)+(3*9)+(2*0)+(1*6)=263
263 % 10 = 3
So 897599-06-3 is a valid CAS Registry Number.

897599-06-3Relevant articles and documents

Synthetic studies of fisetin, myricetin and nobiletin analogs and related probe molecules

Hiza, Aiki,Tsukaguchi, Yuta,Ogawa, Takahiro,Inai, Makoto,Asakawa, Tomohiro,Hamashima, Yoshitaka,Kan, Toshiyuki

, p. 1371 - 1396 (2016/10/12)

We synthesized a series of analogs of fisetin, myricetin and nobiletin, as well as related fluorescein- and biotin-based flavone-probe molecules, on a suitable scale for biological and structure-activity relationship studies.

Concise synthesis of chafurosides A and B

Furuta, Takumi,Nakayama, Miho,Suzuki, Hirotaka,Tajimi, Hiroko,Inai, Makoto,Nukaya, Haruo,Wakimoto, Toshiyuki,Kan, Toshiyuki

supporting information; experimental part, p. 2233 - 2236 (2009/10/02)

The regioselective synthesis of chafurosides A (1) and B (2) from the same methyl ketone 5 was accomplished using a novel protecting group strategy. Both flavone rings were constructed from β-diketone intermediate 4, which was readily obtained by condensation of an acyl donor and ketone 5. Construction of the dihydrofuran ring was achieved via an intramolecular Mitsunobu reaction.

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