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302776-69-8

Benzoic acid, 2-[4-(dibutylamino)-2-hydroxybenzoyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 302776-69-8 Structure

  • Basic information

    1. Product Name: Benzoic acid, 2-[4-(dibutylamino)-2-hydroxybenzoyl]-, methyl ester
    2. Synonyms:
    3. CAS NO:302776-69-8
    4. Molecular Formula: C23H29NO4
    5. Molecular Weight: 383.488
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 302776-69-8.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: Benzoic acid, 2-[4-(dibutylamino)-2-hydroxybenzoyl]-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 2-[4-(dibutylamino)-2-hydroxybenzoyl]-, methyl ester(302776-69-8)
    11. EPA Substance Registry System: Benzoic acid, 2-[4-(dibutylamino)-2-hydroxybenzoyl]-, methyl ester(302776-69-8)

  • 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: 302776-69-8(Hazardous Substances Data)

302776-69-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 302776-69-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,7,7 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 302776-69:
(8*3)+(7*0)+(6*2)+(5*7)+(4*7)+(3*6)+(2*6)+(1*9)=138
138 % 10 = 8
So 302776-69-8 is a valid CAS Registry Number.

302776-69-8Downstream Products

302776-69-8Relevant articles and documents

Catalytic methyl transfer from dimethylcarbonate to carboxylic acids

Ji, Yuan,Sweeney, Jessica,Zoglio, Jillian,Gorin, David J.

, p. 11606 - 11611 (2013)

Although methylation reactions are commonplace, currently used reagents are hazardous, toxic, and/or unstable. Dimethylcarbonate has been put forth as an inexpensive, nontoxic, and green potential methylating reagent. Herein we report a general, base-catalyzed methyl transfer from dimethylcarbonate to carboxylic acids. High selectivity for esterification is observed even in the presence of unprotected phenols, and the mild reaction conditions enable conservation of stereochemistry at epimerizable stereocenters. Isotope-labeling studies suggest a mechanism proceeding by direct methyl transfer from dimethylcarbonate to the substrate.

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