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191603-97-1

1-[2-(3-butenyl)-1-cyclohexenyl]-2(E)-nonen-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 191603-97-1 Structure

  • Basic information

    1. Product Name: 1-[2-(3-butenyl)-1-cyclohexenyl]-2(E)-nonen-1-one
    2. Synonyms: 1-[2-(3-butenyl)-1-cyclohexenyl]-2(E)-nonen-1-one
    3. CAS NO:191603-97-1
    4. Molecular Formula:
    5. Molecular Weight: 274.447
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 191603-97-1.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: 1-[2-(3-butenyl)-1-cyclohexenyl]-2(E)-nonen-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[2-(3-butenyl)-1-cyclohexenyl]-2(E)-nonen-1-one(191603-97-1)
    11. EPA Substance Registry System: 1-[2-(3-butenyl)-1-cyclohexenyl]-2(E)-nonen-1-one(191603-97-1)

  • 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: 191603-97-1(Hazardous Substances Data)

191603-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 191603-97-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,6,0 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 191603-97:
(8*1)+(7*9)+(6*1)+(5*6)+(4*0)+(3*3)+(2*9)+(1*7)=141
141 % 10 = 1
So 191603-97-1 is a valid CAS Registry Number.

191603-97-1Downstream Products

191603-97-1Relevant articles and documents

Total Synthesis of (+/-)-Cylindricines A and B

Fields, Julie,Heathcock, Clayton H.

, p. 8263 - 8266 (2007/10/03)

Cylindricine A (1) and cylindricine B (2) have been aynthesized in 11 steps and 19 percent overall yield. The key reaction involves the addition of an organocopper species to a bicyclic vinylogous amide, which provides complete stereocontrol over the installation of the hexyl side chain.

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