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143266-72-2

2-Furanmethanol, 5-[(dimethylamino)methyl]-4-methyl-a-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 143266-72-2 Structure

  • Basic information

    1. Product Name: 2-Furanmethanol, 5-[(dimethylamino)methyl]-4-methyl-a-phenyl-
    2. Synonyms:
    3. CAS NO:143266-72-2
    4. Molecular Formula: C15H19NO2
    5. Molecular Weight: 245.321
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 143266-72-2.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-Furanmethanol, 5-[(dimethylamino)methyl]-4-methyl-a-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Furanmethanol, 5-[(dimethylamino)methyl]-4-methyl-a-phenyl-(143266-72-2)
    11. EPA Substance Registry System: 2-Furanmethanol, 5-[(dimethylamino)methyl]-4-methyl-a-phenyl-(143266-72-2)

  • 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: 143266-72-2(Hazardous Substances Data)

143266-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143266-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,6 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 143266-72:
(8*1)+(7*4)+(6*3)+(5*2)+(4*6)+(3*6)+(2*7)+(1*2)=122
122 % 10 = 2
So 143266-72-2 is a valid CAS Registry Number.

143266-72-2Downstream Products

143266-72-2Relevant articles and documents

Rearrangement of Dimethyl(furylmethyl)ammonium and Dimethyl(thienylmethyl)ammonium N-Methylides. Isolation and Reaction of Nonaromatic Intermediates

Usami, Takeshi,Shirai, Naohiro,Sato, Yoshiro

, p. 5419 - 5425 (1992)

3--2-methylene-2,3-dihydrofuran (5o) and 2--3-methylene-2,3-dihydrofuran (12o) and their thiophene analogues 5s and 12s were prepared in high yields by fluoride-ion induced desilylation of N,N-dimethyl-N-(2-furylmethyl)ammonium (3o) and -(3-furylmethyl)ammonium iodides (10o) and their thienylmethyl analogues 3s and 10s.Compound 5s or 12s was successfully converted to 3-(2-thienylmethyl)lithium (23s) or 2-(3-thienylmethyl)lithium (26s), which reacted with aldehydes to give (2-hydroxyalkyl)thiophenes 25s or 27s, respectively.

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