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5-Cycloheptene-1,3-diol, 4-ethyl-, (1S,3R,4S)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 669078-51-7 Structure
  • Basic information

    1. Product Name: 5-Cycloheptene-1,3-diol, 4-ethyl-, (1S,3R,4S)- (9CI)
    2. Synonyms: 5-Cycloheptene-1,3-diol, 4-ethyl-, (1S,3R,4S)- (9CI)
    3. CAS NO:669078-51-7
    4. Molecular Formula: C9H16O2
    5. Molecular Weight: 156.22214
    6. EINECS: N/A
    7. Product Categories: ALCOHOL
    8. Mol File: 669078-51-7.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: 5-Cycloheptene-1,3-diol, 4-ethyl-, (1S,3R,4S)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Cycloheptene-1,3-diol, 4-ethyl-, (1S,3R,4S)- (9CI)(669078-51-7)
    11. EPA Substance Registry System: 5-Cycloheptene-1,3-diol, 4-ethyl-, (1S,3R,4S)- (9CI)(669078-51-7)
  • 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: 669078-51-7(Hazardous Substances Data)

669078-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 669078-51-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,9,0,7 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 669078-51:
(8*6)+(7*6)+(6*9)+(5*0)+(4*7)+(3*8)+(2*5)+(1*1)=207
207 % 10 = 7
So 669078-51-7 is a valid CAS Registry Number.

669078-51-7Downstream Products

669078-51-7Relevant articles and documents

Scope of Palladium-Catalyzed Alkylative Ring Opening

Lautens, Mark,Hiebert, Sheldon

, p. 1437 - 1447 (2004)

We have explored the scope of the palladium-catalyzed nucleophilic ring opening methodology. New highly selective and highly active catalysts have been found for the ring opening of oxabenzonorbornadienes. Employing these catalysts, the addition of variou

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