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94058-89-6

2-Benzoxazolamine, 5-chloro-N-phenyl-N-(2-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 94058-89-6 Structure

  • Basic information

    1. Product Name: 2-Benzoxazolamine, 5-chloro-N-phenyl-N-(2-phenylethyl)-
    2. Synonyms:
    3. CAS NO:94058-89-6
    4. Molecular Formula: C21H17ClN2O
    5. Molecular Weight: 348.832
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 94058-89-6.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: 2-Benzoxazolamine, 5-chloro-N-phenyl-N-(2-phenylethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Benzoxazolamine, 5-chloro-N-phenyl-N-(2-phenylethyl)-(94058-89-6)
    11. EPA Substance Registry System: 2-Benzoxazolamine, 5-chloro-N-phenyl-N-(2-phenylethyl)-(94058-89-6)

  • 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: 94058-89-6(Hazardous Substances Data)

94058-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94058-89-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,5 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94058-89:
(7*9)+(6*4)+(5*0)+(4*5)+(3*8)+(2*8)+(1*9)=156
156 % 10 = 6
So 94058-89-6 is a valid CAS Registry Number.

94058-89-6Downstream Products

94058-89-6Relevant articles and documents

A New Method for the Preparation of 2-(Alkylamino)benzoxazoles and 2-(Alkylimino)benzoxazolines

Yamato, Masatoshi,Takeuchi, Yasuo,Hattori, Kyoko,Hashigaki, Kuniko

, p. 3053 - 3060 (2007/10/02)

New syntheses of 2-(alkylamino)benzoxazoles (III) and 3-alkyl-2-(alkylimino)benzoxazolines (IV) were developed.Various compounds III were obtained by the reaction of 2-(methylthio)benzoxazole with amines.In the alkylation of 2-(monoalkylamino)benzoxazoles, the use of a base as a catalyst was found to be important for the selective preparation of 2-(N,N-dialkylamino)benzoxazoles; in the absence of base, IV was obtained.On the other hand, alkylation of N,N'-dialkyl-N-(2-hydroxyphenyl)thioureas resulted in the development of another method for the preparation of IV.Keywords - 2-(alkylamino)benzoxazole; 3-alkyl-2-(alkylimino)benzoxazoline; 2-(methylthio)benzoxazole; N,N'-dialkyl-N-(2-hydroxyphenyl)thiourea; 3-alkylbenzoxazoline-2-thione

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