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ethyl 5-oxocyclooctanecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 122898-08-2 Structure
  • Basic information

    1. Product Name: ethyl 5-oxocyclooctanecarboxylate
    2. Synonyms:
    3. CAS NO:122898-08-2
    4. Molecular Formula:
    5. Molecular Weight: 198.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122898-08-2.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 5-oxocyclooctanecarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 5-oxocyclooctanecarboxylate(122898-08-2)
    11. EPA Substance Registry System: ethyl 5-oxocyclooctanecarboxylate(122898-08-2)
  • 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: 122898-08-2(Hazardous Substances Data)

122898-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122898-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,8,9 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 122898-08:
(8*1)+(7*2)+(6*2)+(5*8)+(4*9)+(3*8)+(2*0)+(1*8)=142
142 % 10 = 2
So 122898-08-2 is a valid CAS Registry Number.

122898-08-2Downstream Products

122898-08-2Relevant articles and documents

Synthesis of 3- and 4-Substituted Cyclic α-Amino Acids Structurally Related to ACPD

Alonso, Francisco,Mico, Irene,Najera, Carmen,Sansano, Jose M.,Yus, Miguel,et al.

, p. 10259 - 10280 (2007/10/02)

The preparation of 3-substituted cyclopentanones 12-16, 4-substituted cyclohexanones 23-28 and cycloheptanones 38-41 is described.Substituents in the cycloalkanones are carboxylate, phosphonate or tetrazole groups, separated from the ring by a 0, 1, 2, or 3 carbon atoms chain.These cycloalkanones have been transformed into α-amino acids 9-11 by hydrolysis of the corresponding hydantoin derivatives 21, 37 and 62, obtained under Bucherer-Bergs reaction conditions.

NOVEL FREE RADICAL RING-EXPANSION REACTIONS

Dowd, Paul,Choi, Soo-Chang

, p. 77 - 90 (2007/10/02)

A novel free radical initiated ring expansion of haloalkyl β-keto esters is described.Following alkylation of the β-keto ester with the appropriate dihalide, the resulting halide is treated at reflux with tri-n-butyltin hydride.Rearrangement to the homolo

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