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1-(Butoxy-phenyl-methyl)-1H-benzotriazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 202396-03-0 Structure
  • Basic information

    1. Product Name: 1-(Butoxy-phenyl-methyl)-1H-benzotriazole
    2. Synonyms:
    3. CAS NO:202396-03-0
    4. Molecular Formula:
    5. Molecular Weight: 281.357
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 202396-03-0.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-(Butoxy-phenyl-methyl)-1H-benzotriazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(Butoxy-phenyl-methyl)-1H-benzotriazole(202396-03-0)
    11. EPA Substance Registry System: 1-(Butoxy-phenyl-methyl)-1H-benzotriazole(202396-03-0)
  • 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: 202396-03-0(Hazardous Substances Data)

202396-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 202396-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,3,9 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 202396-03:
(8*2)+(7*0)+(6*2)+(5*3)+(4*9)+(3*6)+(2*0)+(1*3)=100
100 % 10 = 0
So 202396-03-0 is a valid CAS Registry Number.

202396-03-0Relevant articles and documents

Synthesis of β-Alkoxy Ketones and α′-Functionalized β-Alkoxy Ketones Utilizing Benzotriazole-Stabilized Acyl Anion Synthons

Katritzky, Alan R.,Feng, Darning,Qi, Ming

, p. 1473 - 1477 (1998)

1-(α-Alkoxyalkyl)benzotriazoles 1a-d add to phenyl vinyl ether to form key intermediates 4a-d, which readily undergo lithiation and subsequent trapping by a variety of electrophiles to give the expected substituted derivatives 7a-d, 9a-c, 11, 13, 15, and 18 in high yields. Subsequent hydrolysis of these compounds provides a novel high-yield acyl anion synthon approach for the synthesis of β-alkoxy ketones 8 or α′-functionalized β-alkoxy ketones 10, 12, 14, 16, and 19 by short procedures from readily available starting materials.

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