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180293-71-4

Cycloheptanol, 2,2-diethoxy-, (+)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 180293-71-4 Structure

  • Basic information

    1. Product Name: Cycloheptanol, 2,2-diethoxy-, (+)- (9CI)
    2. Synonyms:
    3. CAS NO:180293-71-4
    4. Molecular Formula: C11H22O3
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: ETHOXY
    8. Mol File: 180293-71-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Cycloheptanol, 2,2-diethoxy-, (+)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cycloheptanol, 2,2-diethoxy-, (+)- (9CI)(180293-71-4)
    11. EPA Substance Registry System: Cycloheptanol, 2,2-diethoxy-, (+)- (9CI)(180293-71-4)

  • 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: 180293-71-4(Hazardous Substances Data)

180293-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180293-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,2,9 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 180293-71:
(8*1)+(7*8)+(6*0)+(5*2)+(4*9)+(3*3)+(2*7)+(1*1)=134
134 % 10 = 4
So 180293-71-4 is a valid CAS Registry Number.

180293-71-4Downstream Products

180293-71-4Relevant articles and documents

Mn-salen catalyzed asymmetric oxidation of enol derivatives

Fukuda, Tsutomu,Katsuki, Tsutomu

, p. 4389 - 4392 (2007/10/03)

Mn-salen complex 1 was found to catalyze highly enantioselective oxidation of enol ethers with iodosylbenzene as a terminal oxidant giving the corresponding hydroxy acetals, when the reaction was carried out in an alcoholic solvent. The reactions in the u

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