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134414-99-6

methyl 2-t-butyl-3-(o-anisyl)-3-hydroxypropionate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134414-99-6 Structure

  • Basic information

    1. Product Name: methyl 2-t-butyl-3-(o-anisyl)-3-hydroxypropionate
    2. Synonyms:
    3. CAS NO:134414-99-6
    4. Molecular Formula:
    5. Molecular Weight: 266.337
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134414-99-6.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: methyl 2-t-butyl-3-(o-anisyl)-3-hydroxypropionate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-t-butyl-3-(o-anisyl)-3-hydroxypropionate(134414-99-6)
    11. EPA Substance Registry System: methyl 2-t-butyl-3-(o-anisyl)-3-hydroxypropionate(134414-99-6)

  • 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: 134414-99-6(Hazardous Substances Data)

134414-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134414-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,4,1 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 134414-99:
(8*1)+(7*3)+(6*4)+(5*4)+(4*1)+(3*4)+(2*9)+(1*9)=116
116 % 10 = 6
So 134414-99-6 is a valid CAS Registry Number.

134414-99-6Downstream Products

134414-99-6Relevant articles and documents

Aldol addition reaction of a lithium ester enolate in the solid state

Wei,Bakthavatchalam

, p. 1535 - 1538 (1991)

The first solid state aldol addition of the lithium enolate of methyl 3,3-dimethylbutanoate to aromatic aldehydes is reported. The diastereoselectivity of the reactions in the solid state is similar to that in solution, suggesting that the same reacting species and transition states might be involved.

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