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ethyl 2,4-dioxocyclohexane-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 77548-33-5 Structure
  • Basic information

    1. Product Name: ethyl 2,4-dioxocyclohexane-1-carboxylate
    2. Synonyms: ethyl 2,4-dioxocyclohexane-1-carboxylate
    3. CAS NO:77548-33-5
    4. Molecular Formula:
    5. Molecular Weight: 184.192
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 77548-33-5.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: ethyl 2,4-dioxocyclohexane-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2,4-dioxocyclohexane-1-carboxylate(77548-33-5)
    11. EPA Substance Registry System: ethyl 2,4-dioxocyclohexane-1-carboxylate(77548-33-5)
  • 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: 77548-33-5(Hazardous Substances Data)

77548-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77548-33-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,4 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77548-33:
(7*7)+(6*7)+(5*5)+(4*4)+(3*8)+(2*3)+(1*3)=165
165 % 10 = 5
So 77548-33-5 is a valid CAS Registry Number.

77548-33-5Downstream Products

77548-33-5Relevant articles and documents

Enantioselective Total Synthesis of Cannogenol-3-O-α- l -rhamnoside via Sequential Cu(II)-Catalyzed Michael Addition/Intramolecular Aldol Cyclization Reactions

Bhattarai, Bijay,Nagorny, Pavel

, p. 154 - 157 (2018)

A concise and scalable enantioselective total synthesis of the natural cardenolides cannogenol and cannogenol-3-O-α-l-rhamnoside has been achieved in 18 linear steps. The synthesis features a Cu(II)-catalyzed enantioselective and diastereoselective Michae

An efficient synthesis of 3-alkyl-1,5,3-dioxazepanes and their use as electrophiles in double-Mannich reactions

Sparrow, Kevin,Barker, David,Brimble, Margaret A.

experimental part, p. 1017 - 1028 (2012/02/13)

An efficient synthesis of 3-alkyl 1,5,3-dioxazepanes was developed for subsequent use in double-Mannich reactions with a variety of carbon-based nucleophiles. It was found that addition of methyltrichlorosilane to the dioxazepane led to a long-lasting rea

N-UREIDOALKYL-AMINO COMPOUNDS AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY

-

, (2008/06/13)

The present application describes modulators of chemokine receptors of formula (I), or pharmaceutically acceptable salt forms thereof, useful for the prevention of asthma and other allergic diseases.

N-ureidoalkyl-piperidines as modulators of chemokine receptor activity

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Page 29, (2008/06/13)

The present application describes modulators of chemokine receptor activity of formula (I): or pharmaceutically acceptable salt forms thereof, useful for the prevention of asthma and other allergic diseases, as well as autoimmune pathologies such as rheum

Zeolite mediated Michael addition of 1,3-dicarbonyl compounds and thiols

Sreekumar,Rugmini,Padmakumar, Raghavakaimal

, p. 6557 - 6560 (2007/10/03)

Zeolites, an environmentally attractive solid catalyst, proves to be an efficient catalyst for Michael addition of several 1,3-dicarbonyl compounds and thiols as donors with methyl vinyl ketone, acrolein and methyl acrylate as acceptors without any solvent are described.

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