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93799-43-0

mandelic acid N-hydroxysuccinimido ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93799-43-0 Structure

  • Basic information

    1. Product Name: mandelic acid N-hydroxysuccinimido ester
    2. Synonyms: mandelic acid N-hydroxysuccinimido ester
    3. CAS NO:93799-43-0
    4. Molecular Formula:
    5. Molecular Weight: 249.223
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93799-43-0.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: mandelic acid N-hydroxysuccinimido ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: mandelic acid N-hydroxysuccinimido ester(93799-43-0)
    11. EPA Substance Registry System: mandelic acid N-hydroxysuccinimido ester(93799-43-0)

  • 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: 93799-43-0(Hazardous Substances Data)

93799-43-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93799-43-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,9 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93799-43:
(7*9)+(6*3)+(5*7)+(4*9)+(3*9)+(2*4)+(1*3)=190
190 % 10 = 0
So 93799-43-0 is a valid CAS Registry Number.

93799-43-0Relevant articles and documents

Preparation method of N,N-diethyl-2-hydroxyl-2-phenylacetamide

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Paragraph 0104; 0105; 0106; 0107-0115, (2019/05/08)

The invention provides a synthesis method of N,N-diethyl-2-hydroxyl-2-phenylacetamide. The N,N-diethyl-2-hydroxyl-2-phenylacetamide is obtained by condensing mandelic acid, serving as a raw material,with N-hydroxysuccinimide, and then performing substitut

Reactions of α-Hydroxy Carbonyl Compounds with Azodicarboxylates and Triphenylphosphine: Synthesis of α-N-Hydroxy Amino Acid Derivatives

Kolasa, Teodozyj,Miller, Marvin J.

, p. 4978 - 4984 (2007/10/02)

Reaction of aliphatic α-hydroxy esters with azodicarboxylates and triphenylphosphine in the presence of either CbzNHOCH2Ph or trOCNHOCH2Ph provides a direct route to protected α-N-hydroxy amino acids.Similar reactions with aromatic α-hydroxy carbonyl compounds and derivatives result in predominate oxidation to the corresponding α-oxo carbonyl derivatives.

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