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CAS

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1141487-32-2

2-(4-acetoxyphenyl)-8-(3-methylbut-2-enyl)-4-oxochroman-5,7-diyl diacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1141487-32-2 Structure

  • Basic information

    1. Product Name: 2-(4-acetoxyphenyl)-8-(3-methylbut-2-enyl)-4-oxochroman-5,7-diyl diacetate
    2. Synonyms: 2-(4-acetoxyphenyl)-8-(3-methylbut-2-enyl)-4-oxochroman-5,7-diyl diacetate
    3. CAS NO:1141487-32-2
    4. Molecular Formula:
    5. Molecular Weight: 466.488
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1141487-32-2.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: 2-(4-acetoxyphenyl)-8-(3-methylbut-2-enyl)-4-oxochroman-5,7-diyl diacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-acetoxyphenyl)-8-(3-methylbut-2-enyl)-4-oxochroman-5,7-diyl diacetate(1141487-32-2)
    11. EPA Substance Registry System: 2-(4-acetoxyphenyl)-8-(3-methylbut-2-enyl)-4-oxochroman-5,7-diyl diacetate(1141487-32-2)

  • 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: 1141487-32-2(Hazardous Substances Data)

1141487-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1141487-32-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,1,4,8 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1141487-32:
(9*1)+(8*1)+(7*4)+(6*1)+(5*4)+(4*8)+(3*7)+(2*3)+(1*2)=132
132 % 10 = 2
So 1141487-32-2 is a valid CAS Registry Number.

1141487-32-2Downstream Products

1141487-32-2Relevant articles and documents

A practical access to highly enantiomerically pure flavanones by catalytic asymmetric transfer hydrogenation

Lemke, Marie-Kristin,Schwab, Pia,Fischer, Petra,Tischer, Sandra,Witt, Morris,Noehringer, Laurence,Rogachev, Victor,Jaeger, Anne,Kataeva, Olga,Froehlich, Roland,Metz, Peter

, p. 11651 - 11655 (2013/11/06)

A surprisingly selective, non-enzymatic kinetic resolution of readily available, racemic β-chiral ketones enabled the title process, which was applied to a rapid synthesis of several bioactive flavanones in virtually enantiopure form (see scheme; MOM=methoxymethyl, Ts=p-toluenesulfonyl). Copyright

An efficient method for C8-prenylation of flavonols and flavanones

Kawamura, Tomoyuki,Hayashi, Moemi,Mukai, Rie,Terao, Junji,Nemoto, Hisao

, p. 1308 - 1314 (2012/06/30)

Synthesis of C8-prenylated flavonols and flavanones via the palladium-catalyzed 7-O-1,1-dimethylprop-2-enylation, followed by Claisen rearrangement is described. Two regioselectivities (carbon-carbon bond formation at either the tail or head of the prenyl

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