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CAS

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438553-16-3

1-[4-(4,4-dimethyloxazolin-2-yl)-5-phenyloxazol-2-yl]-1-phenylmethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 438553-16-3 Structure

  • Basic information

    1. Product Name: 1-[4-(4,4-dimethyloxazolin-2-yl)-5-phenyloxazol-2-yl]-1-phenylmethanol
    2. Synonyms: 1-[4-(4,4-dimethyloxazolin-2-yl)-5-phenyloxazol-2-yl]-1-phenylmethanol
    3. CAS NO:438553-16-3
    4. Molecular Formula:
    5. Molecular Weight: 348.401
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 438553-16-3.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: 1-[4-(4,4-dimethyloxazolin-2-yl)-5-phenyloxazol-2-yl]-1-phenylmethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[4-(4,4-dimethyloxazolin-2-yl)-5-phenyloxazol-2-yl]-1-phenylmethanol(438553-16-3)
    11. EPA Substance Registry System: 1-[4-(4,4-dimethyloxazolin-2-yl)-5-phenyloxazol-2-yl]-1-phenylmethanol(438553-16-3)

  • 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: 438553-16-3(Hazardous Substances Data)

438553-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 438553-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,8,5,5 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 438553-16:
(8*4)+(7*3)+(6*8)+(5*5)+(4*5)+(3*3)+(2*1)+(1*6)=163
163 % 10 = 3
So 438553-16-3 is a valid CAS Registry Number.

438553-16-3Relevant articles and documents

Metalation of 4-oxazolinyloxazole derivatives. A convenient route to 2,4-bifunctionalized oxazoles.

Couture, Axel,Grandclaudon, Pierre,Hoarau, Christophe,Cornet, Josephine,Henichart, Jean-Pierre,Houssin, Raymond

, p. 3601 - 3606 (2007/10/03)

The synthesis of an array of 5-phenyloxazole derivatives bearing a variety of hydroxyalkyl groups at the C-2 position of the heterocyclic nucleus and possessing a formyl or a carboxyl function at C-4 is reported. These bifunctionalized compounds have been efficiently prepared by addition of carbonylated electrophiles to the 2-lithio derivative of 5-phenyloxazole preliminarily equipped with an oxazoline unit at the 4-position of the oxazole nucleus. It is demonstrated that this protocol offers a double advantage since it suppresses the troublesome electrocyclic ring-opening reaction and allows access to the target compounds by simple chemical transformation of the oxazoline ring system.

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