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CAS

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1408236-67-8

4,4,4-trifluoro-1,3-bis(3-hydroxy-4-methylphenyl)butan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1408236-67-8 Structure

  • Basic information

    1. Product Name: 4,4,4-trifluoro-1,3-bis(3-hydroxy-4-methylphenyl)butan-1-one
    2. Synonyms: 4,4,4-trifluoro-1,3-bis(3-hydroxy-4-methylphenyl)butan-1-one
    3. CAS NO:1408236-67-8
    4. Molecular Formula:
    5. Molecular Weight: 338.326
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1408236-67-8.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: 4,4,4-trifluoro-1,3-bis(3-hydroxy-4-methylphenyl)butan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,4,4-trifluoro-1,3-bis(3-hydroxy-4-methylphenyl)butan-1-one(1408236-67-8)
    11. EPA Substance Registry System: 4,4,4-trifluoro-1,3-bis(3-hydroxy-4-methylphenyl)butan-1-one(1408236-67-8)

  • 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: 1408236-67-8(Hazardous Substances Data)

1408236-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1408236-67-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,8,2,3 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1408236-67:
(9*1)+(8*4)+(7*0)+(6*8)+(5*2)+(4*3)+(3*6)+(2*6)+(1*7)=148
148 % 10 = 8
So 1408236-67-8 is a valid CAS Registry Number.

1408236-67-8Downstream Products

1408236-67-8Relevant articles and documents

Efficient synthesis of trifluoromethylated dihydrochalcones, aryl vinyl ketones and indanones by superelectrophilic activation of 4,4,4-trifluoro/3- (trifluoromethyl)crotonic acids

Surya Prakash,Paknia, Farzaneh,Narayanan, Arjun,Rasul, Golam,Mathew, Thomas,Olah, George A.

, p. 292 - 302 (2013/01/13)

Superacid catalyzed electrophilic substitution of arenes using 4,4,4,-trifluoro/3-trifluoromethylcrotonic acids has been investigated. The direct synthesis of various trifluoromethylated dihydrochalcones, aryl vinyl ketones and indanones has been achieved by this methodology. It has been found that the position of the trifluoromethyl group has a profound effect on the nature of the reaction and the products. In the pharmaceutical industry, many fluoroorganics are shown to possess significant biological and therapeutic activities. Therefore, these novel compounds can be considered key intermediates for the preparation of potential biologically active molecules.

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