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729569-76-0

methyl 3-[tert-butyl(dimethyl)silyl]oxy-5-(hydroxymethyl)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 729569-76-0 Structure

  • Basic information

    1. Product Name: methyl 3-[tert-butyl(dimethyl)silyl]oxy-5-(hydroxymethyl)benzoate
    2. Synonyms: methyl 3-[tert-butyl(dimethyl)silyl]oxy-5-(hydroxymethyl)benzoate
    3. CAS NO:729569-76-0
    4. Molecular Formula:
    5. Molecular Weight: 296.439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 729569-76-0.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: methyl 3-[tert-butyl(dimethyl)silyl]oxy-5-(hydroxymethyl)benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 3-[tert-butyl(dimethyl)silyl]oxy-5-(hydroxymethyl)benzoate(729569-76-0)
    11. EPA Substance Registry System: methyl 3-[tert-butyl(dimethyl)silyl]oxy-5-(hydroxymethyl)benzoate(729569-76-0)

  • 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: 729569-76-0(Hazardous Substances Data)

729569-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 729569-76-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,9,5,6 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 729569-76:
(8*7)+(7*2)+(6*9)+(5*5)+(4*6)+(3*9)+(2*7)+(1*6)=220
220 % 10 = 0
So 729569-76-0 is a valid CAS Registry Number.

729569-76-0Relevant articles and documents

Synthesis and properties of new, spatially relaxed dendrons containing internal carboxyl groups

Kikuzawa, Yoshihiro,Nagata, Toshi

, p. 993 - 1000 (2004)

We synthesized a series of new dendrons with up to fourteen internal carboxyl groups. These dendrons are made from a branching unit and a spacer unit with a carboxyl group. The growth reactions (formation of the benzylic ether bonds) are completed within

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