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phenyl 4,4,4-trifluoro-3-hydroxy-3-(4-methoxyphenyl)butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1369922-71-3 Structure
  • Basic information

    1. Product Name: phenyl 4,4,4-trifluoro-3-hydroxy-3-(4-methoxyphenyl)butanoate
    2. Synonyms: phenyl 4,4,4-trifluoro-3-hydroxy-3-(4-methoxyphenyl)butanoate
    3. CAS NO:1369922-71-3
    4. Molecular Formula:
    5. Molecular Weight: 340.299
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1369922-71-3.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: phenyl 4,4,4-trifluoro-3-hydroxy-3-(4-methoxyphenyl)butanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenyl 4,4,4-trifluoro-3-hydroxy-3-(4-methoxyphenyl)butanoate(1369922-71-3)
    11. EPA Substance Registry System: phenyl 4,4,4-trifluoro-3-hydroxy-3-(4-methoxyphenyl)butanoate(1369922-71-3)
  • 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: 1369922-71-3(Hazardous Substances Data)

1369922-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1369922-71-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,9,9,2 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1369922-71:
(9*1)+(8*3)+(7*6)+(6*9)+(5*9)+(4*2)+(3*2)+(2*7)+(1*1)=203
203 % 10 = 3
So 1369922-71-3 is a valid CAS Registry Number.

1369922-71-3Downstream Products

1369922-71-3Relevant articles and documents

Convenient and efficient decarboxylative aldol reaction of malonic acid half esters with trifluoromethyl ketones

Li, Xiao-Juan,Xiong, Heng-Ying,Hua, Ming-Qing,Nie, Jing,Zheng, Yan,Ma, Jun-An

, p. 2117 - 2120 (2012)

A convenient and efficient decarboxylative ketone aldol condensation of malonic acid half esters was reported. In the presence of catalytic amount of triethylamine, a series of aromatic and alkyl trifluoromethyl ketones were transformed into the desired adducts in 61-99% yields. In a preliminary experiment, a moderate stereoselectivity was obtained. Direct reduction of the aldol product with LiAlH4 afforded trifluoromethylated 1,3-diol.

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