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CAS

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123622-06-0

1-(2-Methyl-1-phenoxy-propyl)-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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  • 123622-06-0 Structure

  • Basic information

    1. Product Name: 1-(2-Methyl-1-phenoxy-propyl)-1H-benzotriazole
    2. Synonyms: 1-(2-Methyl-1-phenoxy-propyl)-1H-benzotriazole
    3. CAS NO:123622-06-0
    4. Molecular Formula:
    5. Molecular Weight: 267.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123622-06-0.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-(2-Methyl-1-phenoxy-propyl)-1H-benzotriazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-Methyl-1-phenoxy-propyl)-1H-benzotriazole(123622-06-0)
    11. EPA Substance Registry System: 1-(2-Methyl-1-phenoxy-propyl)-1H-benzotriazole(123622-06-0)

  • 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: 123622-06-0(Hazardous Substances Data)

123622-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123622-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,6,2 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 123622-06:
(8*1)+(7*2)+(6*3)+(5*6)+(4*2)+(3*2)+(2*0)+(1*6)=90
90 % 10 = 0
So 123622-06-0 is a valid CAS Registry Number.

123622-06-0Downstream Products

123622-06-0Relevant articles and documents

Reactions of 1-(α-Alkoxyalkyl)- and 1-(α-(Aryloxy)alkyl)benzotriazoles with the Grignard Reagents. A New and Versatile Method for the Preparation of Ethers

Katritzky, Alan R.,Rachwal, Stanislaw,Rachwal, Bogumila

, p. 6022 - 6029 (1989)

1-(α-Alkoxyalkyl)benzotriazoles deriving from aldehydes (other than formaldehyde), or from ketones, react with Grignard reagents at 110 deg C to provide a high-yielding, general synthesis of dialkyl and aryl ethers.Under similar conditions, 1-(alkoxymethyl)- and 1-((aryloxy)methyl)benzotriazoles give, by a different cleavage pattern of the N-C-O grouping, 1-alkylbenzotriazoles and N,N'-dialkyl-o-phenylenediamines.The 1-(α-alkoxyalkyl)benzotriazoles are easily prepared: (a) by condensation of benzotriazole, an aldehyde, and an alcohol under water-removing conditions; (b) by condensation of a 1-(α-chloroalkyl)benzotriazole with a sodium or potassium alkoxide or aryloxide; and (c) by condensatioon of an acetal or a ketal with benzotriazole.All the 1-(α-alkoxyalkyl)benzotriazoles and dialkyl or alkyl aryl ethers obtained were fully characterized by their 1H and 13C NMR spectra.

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