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92684-01-0

2-Oxoglutarsaeure-1-methylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92684-01-0 Structure

  • Basic information

    1. Product Name: 2-Oxoglutarsaeure-1-methylester
    2. Synonyms: 2-Oxoglutarsaeure-1-methylester
    3. CAS NO:92684-01-0
    4. Molecular Formula:
    5. Molecular Weight: 160.127
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92684-01-0.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-Oxoglutarsaeure-1-methylester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Oxoglutarsaeure-1-methylester(92684-01-0)
    11. EPA Substance Registry System: 2-Oxoglutarsaeure-1-methylester(92684-01-0)

  • 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: 92684-01-0(Hazardous Substances Data)

92684-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92684-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,6,8 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92684-01:
(7*9)+(6*2)+(5*6)+(4*8)+(3*4)+(2*0)+(1*1)=150
150 % 10 = 0
So 92684-01-0 is a valid CAS Registry Number.

92684-01-0Downstream Products

92684-01-0Relevant articles and documents

Organic Syntheses Based on 2-Oxoglutaric Acid. II. On the Synthesis of Heterocycles by Reactions of Dimethyl 3-bromo-2-oxoglutarate with Binucleophiles

Hartenstein, H.,Blitzke, T.,Sicker, D.,Wilde, H.

, p. 176 - 180 (1993)

Reactions of dimethyl 3-bromo-2-oxoglutarate 2 with binucleophiles to form heterocycles proceed on two different pathways depending on the type of reactant.Thus, strong S-nucleophiles like thioureas and thiocarbohydrazide substitute initially the bromine atom and form 2-aminothiazoles 3 - 7 and the 1,3,4-thiadiazine 8.However, o-phenylendiamines reacted to form the brominated quinoxaline-2(1H)-one derivatives 9 and 10, resp.

Tricyclic cepham compounds

-

, (2008/06/13)

The compounds having a 4,11-dioxo-3-oxa-8(or 7)-thia-1-azatricyclo[7,2,0,02,6 ]undecane-2-carboxylic acid skeleton as the base structure, their esters and their salts are useful antibacterial agents.

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