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103441-61-8

1-(2-hydroxy-3-iodo-4-methoxyphenyl)ethanone, also known as iodovanillin, is a chemical compound with a molecular formula C9H9IO3. It is a derivative of vanillin, a widely used flavoring agent. Iodovanillin is characterized by a hydroxy group, an iodine atom, and a methoxy group attached to a benzene ring, along with an ethanone functional group. It is utilized in organic synthesis and pharmaceutical research as an intermediate for the preparation of various drugs and pharmaceuticals. It also has potential applications in the field of organic chemistry due to its unique structure and reactivity. However, it is important to handle this chemical with care as it may be harmful if ingested or if it comes into contact with skin or eyes.

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  • 103441-61-8 Structure

  • Basic information

    1. Product Name: 1-(2-hydroxy-3-iodo-4-methoxyphenyl)ethanone
    2. Synonyms: 1-(2-hydroxy-3-iodo-4-methoxyphenyl)ethanone
    3. CAS NO:103441-61-8
    4. Molecular Formula:
    5. Molecular Weight: 292.073
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103441-61-8.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: 1-(2-hydroxy-3-iodo-4-methoxyphenyl)ethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-hydroxy-3-iodo-4-methoxyphenyl)ethanone(103441-61-8)
    11. EPA Substance Registry System: 1-(2-hydroxy-3-iodo-4-methoxyphenyl)ethanone(103441-61-8)

  • 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: 103441-61-8(Hazardous Substances Data)

103441-61-8 Usage

Uses

Used in Pharmaceutical Research:
1-(2-hydroxy-3-iodo-4-methoxyphenyl)ethanone is used as an intermediate in the synthesis of various drugs and pharmaceuticals for its unique reactivity and structural properties.
Used in Organic Synthesis:
1-(2-hydroxy-3-iodo-4-methoxyphenyl)ethanone is used as a key compound in the preparation of complex organic molecules, taking advantage of its unique functional groups and reactivity.
Used in Chemical Research:
1-(2-hydroxy-3-iodo-4-methoxyphenyl)ethanone is used as a research compound to study its properties and potential applications in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 103441-61-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,4,4 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103441-61:
(8*1)+(7*0)+(6*3)+(5*4)+(4*4)+(3*1)+(2*6)+(1*1)=78
78 % 10 = 8
So 103441-61-8 is a valid CAS Registry Number.

103441-61-8Relevant articles and documents

Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels-Alder adducts morusalbanol A and 441772-64-1

Tee, Jia Ti,Chee, Chin Fei,Buckle, Michael J.C.,Lee, Vannajan Sanghiran,Chong, Wei Lim,Khaledi, Hamid,Rahman, Noorsaadah Abd

, p. 5082 - 5085 (2015/08/06)

Preparation of the oxabicyclic [3.3.1] cores of morusalbanol A and 441772-64-1 was achieved via the intramolecular cyclization of cis-trans (endo) mulberry Diels-Alder adducts. The latter were derived from a hydrogen bond-assisted regioselective Diels-Alder reaction between a chalcone dienophile and a dehydroprenyl diene. Results from these studies provide important insights into the syntheses of morusalbanol A and related mulberry Diels-Alder adducts.

Synthetic studies towards the mulberry Diels-Alder adducts: H-bond accelerated cycloadditions of chalcones

Boonsri, Sompong,Gunawan, Christian,Krenske, Elizabeth H.,Rizzacasa, Mark A.

experimental part, p. 6010 - 6021 (2012/08/28)

The methyl ether derivatives 2, 4 and 6 of the mulberry Diels-Alder adducts chalcomoracin (1) and mulberrofuran C (3) and kuwanon J (5) respectively have been synthesized by a thermal [4 + 2]-cycloaddition reaction between a chalcone and dehydroprenyl die

Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor

-

Page/Page column 36, (2010/02/14)

The present invention is directed to compounds of formula (I), which antagonize of the effects of melanin-concentrating hormone (MCH) through the melanin concentrating hormone receptor which is useful for the prevention or treatment of eating disorders, weight gain, obesity, abnormalities in reproduction and sexual behavior, thyroid hormone secretion, diuresis and water/electrolyte homeostasis, sensory processing, memory, sleeping, arousal, anxiety, depression, seizures, neurodegeneration and psychiatric disorders.

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