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CAS

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107699-07-0

2-(2,3-epoxy-2-phenylpropyl)-4-methylthiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107699-07-0 Structure

  • Basic information

    1. Product Name: 2-(2,3-epoxy-2-phenylpropyl)-4-methylthiazole
    2. Synonyms: 2-(2,3-epoxy-2-phenylpropyl)-4-methylthiazole
    3. CAS NO:107699-07-0
    4. Molecular Formula:
    5. Molecular Weight: 231.318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107699-07-0.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: 2-(2,3-epoxy-2-phenylpropyl)-4-methylthiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2,3-epoxy-2-phenylpropyl)-4-methylthiazole(107699-07-0)
    11. EPA Substance Registry System: 2-(2,3-epoxy-2-phenylpropyl)-4-methylthiazole(107699-07-0)

  • 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: 107699-07-0(Hazardous Substances Data)

107699-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107699-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,6,9 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107699-07:
(8*1)+(7*0)+(6*7)+(5*6)+(4*9)+(3*9)+(2*0)+(1*7)=150
150 % 10 = 0
So 107699-07-0 is a valid CAS Registry Number.

107699-07-0Relevant articles and documents

Routes to Pyrrolothiazoles. Rotational Isomerism of Pyrrolo-thiazole-5-carbaldehydes

Brindley, Jocelyn C.,Gillon, David G.,Meakins, Denis G.

, p. 1255 - 1260 (2007/10/02)

Four 3,6-disubstituted pyrrolothiazoles (one containing a 3-aryl group) were prepared from 2,4-disubstituted thiazoles by the known method, and this work clarified some confusion in the literature.A new route, involving substitution into the thiazo

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