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CAS

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1401094-49-2

3-(2-furoyl)hexanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1401094-49-2 Structure

  • Basic information

    1. Product Name: 3-(2-furoyl)hexanal
    2. Synonyms: 3-(2-furoyl)hexanal
    3. CAS NO:1401094-49-2
    4. Molecular Formula:
    5. Molecular Weight: 194.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1401094-49-2.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: 3-(2-furoyl)hexanal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(2-furoyl)hexanal(1401094-49-2)
    11. EPA Substance Registry System: 3-(2-furoyl)hexanal(1401094-49-2)

  • 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: 1401094-49-2(Hazardous Substances Data)

1401094-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1401094-49-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,0,9 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1401094-49:
(9*1)+(8*4)+(7*0)+(6*1)+(5*0)+(4*9)+(3*4)+(2*4)+(1*9)=112
112 % 10 = 2
So 1401094-49-2 is a valid CAS Registry Number.

1401094-49-2Downstream Products

1401094-49-2Relevant articles and documents

Elucidating the formation pathway of the off-flavor compound 6-propylbenzofuran-7-ol

Sakamaki, Kensuke,Ishizaki, Susumu,Ohkubo, Yasutaka,Tateno, Yoshiyuki,Nakanishi, Akira,Fujita, Akira

, p. 9967 - 9973,7 (2020/09/15)

In a previous work, we identified 6-propylbenzofuran-7-ol as an off-flavor compound formed from ascorbic acid and (E)-hex-2-enal in a test apple beverage. In this study, we elucidate the pathway by which 6-propylbenzofuran-7-ol formed. Isotope labeling studies revealed that the propyl group of 6-propylbenzofuran- 7-ol derives from (E)-hex-2-enal and that 6-propylbenzofuran-7-ol contains carbons 2-6 of ascorbic acid. Two compounds, namely, 2,3-dihydro-6- propylbenzofuran-3,7-diol and 3-(2-furoyl)hexanal, were identified as byproducts of a model reaction of ascorbic acid and (E)-hex-2-enal. Each of these compounds was dissolved in an aqueous solution of citric acid and stored at 60 °C for 1 week. After storage, 6-propylbenzofuran-7-ol was detected from a solution of 2,3-dihydro-6-propylbenzofuran-3,7-diol, but not from 3-(2-furoyl)hexanal. 6-Propylbenzofuran-7-ol was formed by isolating tricyclic hemiacetal lactone derived from the Michael addition of ascorbic acid to (E)-hex-2-enal, mixing the tricyclic hemiacetal lactone with the aqueous solution of citric acid, and applying heat. This confirmed that 6-propylbenzofuran-7-ol was formed via the Michael adduct.

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