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2(3H)-Furanone, dihydro-4-(hydroxymethyl)-3-(1-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 143994-26-7 Structure
  • Basic information

    1. Product Name: 2(3H)-Furanone, dihydro-4-(hydroxymethyl)-3-(1-phenylethyl)-
    2. Synonyms:
    3. CAS NO:143994-26-7
    4. Molecular Formula: C13H16O3
    5. Molecular Weight: 220.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 143994-26-7.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: 2(3H)-Furanone, dihydro-4-(hydroxymethyl)-3-(1-phenylethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2(3H)-Furanone, dihydro-4-(hydroxymethyl)-3-(1-phenylethyl)-(143994-26-7)
    11. EPA Substance Registry System: 2(3H)-Furanone, dihydro-4-(hydroxymethyl)-3-(1-phenylethyl)-(143994-26-7)
  • 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: 143994-26-7(Hazardous Substances Data)

143994-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143994-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,9,9 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 143994-26:
(8*1)+(7*4)+(6*3)+(5*9)+(4*9)+(3*4)+(2*2)+(1*6)=157
157 % 10 = 7
So 143994-26-7 is a valid CAS Registry Number.

143994-26-7Downstream Products

143994-26-7Relevant articles and documents

Furan-2(3H)- and 2(5H)-ones. Part 5. Photoreaction of 3-Benzylfuran-2(5H)-ones; Cyclisation to Indenofuranones

Muraoka, Osamu,Tanabe, Genzoh,Sano, Kyohko,Minematsu, Toshie,Momose, Takefumi

, p. 1833 - 1846 (2007/10/02)

The effect of substitution at the 'central methane' on the photoreactivity of 3-benzylfuran-2(5H)-ones 5a-g was investigated.Despite its di-?-methane structure, photochemical arylation was effected to give substituted indenofuranones 6 in good yields.Only

A BREAKTHROUGH FOR THE PHOTOCHEMICAL ARYLATION IN THE 3-(PHENYLMETHYL)-2(5H)-FURANONE SYSTEM LEADING TO THE TETRAHYDROINDENOFURANONE SYSTEM

Muraoka, Osamu,Tanabe, Genzoh,Sano, Kyohko,Momose, Takefumi

, p. 1093 - 1096 (2007/10/02)

The photochemistry of the 'central methane'-substituted 3-benzyl-2(5H)-furanone system (1) is described.Despite its di-?-methane structure, photochemical arylation was found to predominate in place of the di-?-methane rearrangement, and gave substituted t

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