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Ethanone, 1-(4-hydroxyphenyl)-2-(4-methoxyphenyl)-, also known as 1-(4-hydroxyphenyl)-2-(4-methoxyphenyl)ethanone or 1-(4-methoxyphenyl)-2-(4-hydroxyphenyl)ethanone, is an organic compound with the molecular formula C15H14O3. It is a derivative of acetophenone, featuring a hydroxyl group (-OH) attached to the 4-position of one phenyl ring and a methoxy group (-OCH3) attached to the 4-position of the other phenyl ring. Ethanone, 1-(4-hydroxyphenyl)-2-(4-methoxyphenyl)- is a white crystalline solid and is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals. It is also used as an intermediate in the production of certain dyes and pigments. Due to its chemical structure, it exhibits properties such as low solubility in water and high solubility in organic solvents.

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  • 3669-46-3 Structure
  • Basic information

    1. Product Name: Ethanone, 1-(4-hydroxyphenyl)-2-(4-methoxyphenyl)-
    2. Synonyms:
    3. CAS NO:3669-46-3
    4. Molecular Formula: C15H14O3
    5. Molecular Weight: 242.274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3669-46-3.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: Ethanone, 1-(4-hydroxyphenyl)-2-(4-methoxyphenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-(4-hydroxyphenyl)-2-(4-methoxyphenyl)-(3669-46-3)
    11. EPA Substance Registry System: Ethanone, 1-(4-hydroxyphenyl)-2-(4-methoxyphenyl)-(3669-46-3)
  • 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: 3669-46-3(Hazardous Substances Data)

3669-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3669-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,6 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3669-46:
(6*3)+(5*6)+(4*6)+(3*9)+(2*4)+(1*6)=113
113 % 10 = 3
So 3669-46-3 is a valid CAS Registry Number.

3669-46-3Relevant articles and documents

1, 2 DISUBSTITUTED HETEROCYCLIC COMPOUNDS

-

, (2010/01/30)

1,2-disubstituted heterocyclic compounds which are inhibitors of phosphodiesterase 10 are described. Also described are processes, pharmaceutical compositions, pharmaceutical preparations and pharmaceutical use of the compounds in the treatment of mammals, including human(s) for central nervous system (CNS) disorders and other disorders which may affect CNS function. Among the disorders which may be treated are neurological, neurodegenerative and psychiatric disorders including, but not limited to, those associated with cognitive deficits or schizophrenic symptoms.

Structure-Activity Relationship of Antiestrogens. Phenolic Analogues of 2,3-Diaryl-2H-1-benzopyrans

Sharma, Arun P.,Saeed, Ashraf,Durani, Susheel,Kapil, Randhir S.

, p. 3222 - 3229 (2007/10/02)

Phenolic analogues of 2--3-phenyl-2H-1-benzopyran (1), a novel antiestrogen, were synthesized and evaluated for their structure-activity relationship.Incorporation of OH at position 7 was found to improve receptor affinity of

Fries Rearrangement of ortho- and para-Methoxy Phenyl Acetates. The formation of Ketoesters

Martin, Robert,Gros, Nicole,Boehmer, Volker,Kaemmerer, Hermann

, p. 81 - 92 (2007/10/02)

During the Fries rearrangement of o- and p-methoxy phenyl acetates with AlCl3 in nitromethane at 20 deg C substitution occurs mainly in the p-position of the phenolic residue to yield p-acylphenols.Larger quantities of o-acylphenols are obtained only, if

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