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83477-99-0

2-hydroxy-3-(benzyloxy)succinimide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83477-99-0 Structure

  • Basic information

    1. Product Name: 2-hydroxy-3-(benzyloxy)succinimide
    2. Synonyms: 2-hydroxy-3-(benzyloxy)succinimide
    3. CAS NO:83477-99-0
    4. Molecular Formula:
    5. Molecular Weight: 221.213
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83477-99-0.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-hydroxy-3-(benzyloxy)succinimide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-hydroxy-3-(benzyloxy)succinimide(83477-99-0)
    11. EPA Substance Registry System: 2-hydroxy-3-(benzyloxy)succinimide(83477-99-0)

  • 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: 83477-99-0(Hazardous Substances Data)

83477-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83477-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,7 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83477-99:
(7*8)+(6*3)+(5*4)+(4*7)+(3*7)+(2*9)+(1*9)=170
170 % 10 = 0
So 83477-99-0 is a valid CAS Registry Number.

83477-99-0Downstream Products

83477-99-0Relevant articles and documents

Enantioselective Syntheses of 3-Substituted 4-(Alkoxycarbonyl)-2-azetidinones from Malic Acid

Miller, Marvin J.,Bajwa, Joginder S.,Mattingly, Phillip G.,Peterson, Kathleen

, p. 4928 - 4933 (2007/10/02)

Enantioselective syntheses of 3-substituted 4-(alkoxycarbonyl)-2-azetidinones from malic acid have been developed.Alkylation of diesters of D-malic acid provided primarily the erythro products 15RS.Base-mediated inversion gave racemic threo isomers 15.Saponification of 15 and selective monoesterification provided the correspondingly substituted β-hydroxy acids 17, which could also be epimerized at the hydroxyl position.Separate conversion of the isomers 17 to the hydroxamates 18 followed by cyclization gave the desired β-lactams 19 with complete control of stereochemistry.

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