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CAS

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843664-51-7

(4S,5S)-4((S)-(but-3-en-2-yl)-2-(4-methoxyphenyl))-5-methyl-1,3-dioxane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 843664-51-7 Structure

  • Basic information

    1. Product Name: (4S,5S)-4((S)-(but-3-en-2-yl)-2-(4-methoxyphenyl))-5-methyl-1,3-dioxane
    2. Synonyms:
    3. CAS NO:843664-51-7
    4. Molecular Formula:
    5. Molecular Weight: 262.349
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 843664-51-7.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: (4S,5S)-4((S)-(but-3-en-2-yl)-2-(4-methoxyphenyl))-5-methyl-1,3-dioxane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,5S)-4((S)-(but-3-en-2-yl)-2-(4-methoxyphenyl))-5-methyl-1,3-dioxane(843664-51-7)
    11. EPA Substance Registry System: (4S,5S)-4((S)-(but-3-en-2-yl)-2-(4-methoxyphenyl))-5-methyl-1,3-dioxane(843664-51-7)

  • 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: 843664-51-7(Hazardous Substances Data)

843664-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 843664-51-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,3,6,6 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 843664-51:
(8*8)+(7*4)+(6*3)+(5*6)+(4*6)+(3*4)+(2*5)+(1*1)=187
187 % 10 = 7
So 843664-51-7 is a valid CAS Registry Number.

843664-51-7Relevant articles and documents

Synthesis of C11-desmethoxy soraphen A1α: A natural product analogue that inhibits acetyl-CoA carboxylase

Canterbury, Daniel P.,Scott, Kristen E. N.,Kubo, Ozora,Jansen, Rolf,Cleveland, John L.,Micalizio, Glenn C.

, p. 1244 - 1248 (2013)

A synthesis of C11-desmethoxy soraphen A1α is described that proceeds in just 14 steps from readily available starting materials. This natural product analogue was identified as a target of interest in a program aimed at identifying novel natural product-inspired inhibitors of acetyl-CoA carboxylase (ACC) as potential anticancer therapeutics. While describing the most efficient synthesis of a soraphen A1α analogue (total syntheses of the natural product have been reported that proceed in 25 to ≥40 linear steps), we also present data supporting the conclusion that C11-heteroatom functionality is a beneficial but unnecessary structural characteristic of soraphen A1α analogues for inhibiting ACC.

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