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CAS

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677313-37-0

Cyclopentene, 4-ethoxy-1-(2-methoxyethyl)-2,3,3-trimethyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 677313-37-0 Structure

  • Basic information

    1. Product Name: Cyclopentene, 4-ethoxy-1-(2-methoxyethyl)-2,3,3-trimethyl- (9CI)
    2. Synonyms: Cyclopentene, 4-ethoxy-1-(2-methoxyethyl)-2,3,3-trimethyl- (9CI)
    3. CAS NO:677313-37-0
    4. Molecular Formula: C13H24O2
    5. Molecular Weight: 212.32846
    6. EINECS: N/A
    7. Product Categories: ETHOXY
    8. Mol File: 677313-37-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 253.2±40.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.91±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Cyclopentene, 4-ethoxy-1-(2-methoxyethyl)-2,3,3-trimethyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclopentene, 4-ethoxy-1-(2-methoxyethyl)-2,3,3-trimethyl- (9CI)(677313-37-0)
    11. EPA Substance Registry System: Cyclopentene, 4-ethoxy-1-(2-methoxyethyl)-2,3,3-trimethyl- (9CI)(677313-37-0)

  • 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: 677313-37-0(Hazardous Substances Data)

677313-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 677313-37-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,7,3,1 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 677313-37:
(8*6)+(7*7)+(6*7)+(5*3)+(4*1)+(3*3)+(2*3)+(1*7)=180
180 % 10 = 0
So 677313-37-0 is a valid CAS Registry Number.

677313-37-0Upstream product

677313-37-0Relevant articles and documents

Synthesis of Chiral Cyclohexenones from α-Campholenic, Fencholenic, and β-Campholenic Derivatives

Anhalt, Katrin,Sprung, Ines,Schulze, Klaus

, p. 1593 - 1606 (2007/10/03)

Optically active dimethylcyclohexenones, potential building blocks for enantioselective syntheses of various naturally active substances, were prepared. These compounds were obtained by oxidation with KMnO 4/Pb(OAc)4 or ozonolysis of the corresponding cyclopentenic precursors, followed by aldol condensation. During the course of the preparation intermediate diols and chiral polyfunctional carbonyl derivatives were separated and identified analytically.

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