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171625-17-5

(S)-6-Benzyloxymethyl-3-isopropoxy-cyclohex-2-enone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • (S)-6-Benzyloxymethyl-3-isopropoxy-cyclohex-2-enone

    Cas No: 171625-17-5

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  • 171625-17-5 Structure

  • Basic information

    1. Product Name: (S)-6-Benzyloxymethyl-3-isopropoxy-cyclohex-2-enone
    2. Synonyms: (S)-6-Benzyloxymethyl-3-isopropoxy-cyclohex-2-enone
    3. CAS NO:171625-17-5
    4. Molecular Formula:
    5. Molecular Weight: 274.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 171625-17-5.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: (S)-6-Benzyloxymethyl-3-isopropoxy-cyclohex-2-enone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-6-Benzyloxymethyl-3-isopropoxy-cyclohex-2-enone(171625-17-5)
    11. EPA Substance Registry System: (S)-6-Benzyloxymethyl-3-isopropoxy-cyclohex-2-enone(171625-17-5)

  • 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: 171625-17-5(Hazardous Substances Data)

171625-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 171625-17-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,6,2 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 171625-17:
(8*1)+(7*7)+(6*1)+(5*6)+(4*2)+(3*5)+(2*1)+(1*7)=125
125 % 10 = 5
So 171625-17-5 is a valid CAS Registry Number.

171625-17-5Upstream product

171625-17-5Relevant articles and documents

Tremorgenic Indole Alkaloids. 9. Asymmetric Construction of an Advanced F-G-H-Ring Lactone Precursor for the Synthesis of Penitrem D

Smith, Amos B.,Nolen, Ernest G.,Shirai, Ryuichi,Blase, Frances R.,Ohta, Mitsuaki,et al.

, p. 7837 - 7848 (2007/10/03)

Lactone (+)-12 is envisioned as the precursor to the F-G-H rings of penitrem D (4) in our ongoing synthetic venture.The efficient, stereocontrolled introduction of the vicinal quaternary methyl groups present the major challenge in the construction of this subunit.Our first route to (+/-)-12 was marked by low overall yield (2percent) and the instability of several key intermediates; these deficiencies were rectified in a second-generation approach that produced optically active material (18 steps from 19a, 2.1percent overall).The successful strategies exploited enolate generation via either conjugate additions to α,β-enones or the Evans oxy-Cope rearrangement as key regiochemical control elements.

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