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460990-43-6

1-(methoxymethyl)-2-(phenylthio)-1H-imidazole-5-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 460990-43-6 Structure

  • Basic information

    1. Product Name: 1-(methoxymethyl)-2-(phenylthio)-1H-imidazole-5-carbaldehyde
    2. Synonyms: 1-(methoxymethyl)-2-(phenylthio)-1H-imidazole-5-carbaldehyde
    3. CAS NO:460990-43-6
    4. Molecular Formula:
    5. Molecular Weight: 248.305
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 460990-43-6.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-(methoxymethyl)-2-(phenylthio)-1H-imidazole-5-carbaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(methoxymethyl)-2-(phenylthio)-1H-imidazole-5-carbaldehyde(460990-43-6)
    11. EPA Substance Registry System: 1-(methoxymethyl)-2-(phenylthio)-1H-imidazole-5-carbaldehyde(460990-43-6)

  • 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: 460990-43-6(Hazardous Substances Data)

460990-43-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 460990-43-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,0,9,9 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 460990-43:
(8*4)+(7*6)+(6*0)+(5*9)+(4*9)+(3*0)+(2*4)+(1*3)=166
166 % 10 = 6
So 460990-43-6 is a valid CAS Registry Number.

460990-43-6Relevant articles and documents

Extending pummerer reaction chemistry: Studies in the palau'amine synthesis area

Feldman, Ken S.,Nuriye, Ahmed Yimam,Li, Jianfeng

, p. 5042 - 5060 (2011/08/06)

Exploratory oxidative cyclization studies on cyclopentanelated and cyclohexenelated oroidin derivatives utilized Pummerer chemistry to generate pentacyclic structures related to the palau'amine family of sponge metabolites. Stereochemical issues were para

Homonuclear Diels-Alder dimerization of 5-ethenyl-2-phenylsulfanyl-1H-imidazoles and its application to synthesis of 12,12′-dimethylageliferin

Kawasaki, Ikuo,Sakaguchi, Norihiro,Khadeer, Abdul,Yamashita, Masayuki,Ohta, Shunsaku

, p. 10182 - 10192 (2007/10/03)

Homonuclear Diels-Alder dimerization of various 5-ethenyl-2-phenylsulfanyl-1H-imidazoles provided a novel highly regio- and stereoselective route to the preparation of multifunctionalized 4,5,6,7-tetrahydrobenzimidazoles, which is the basic skeleton of ag

Novel Diels-Alder-type dimerization of 5-ethenyl-2-phenylsulfanyl-1H-imidazoles and its application to biomimetic synthesis of 12,12′-dimethylageliferin

Kawasaki, Ikuo,Sakaguchi, Norihiro,Fukushima, Norie,Fujioka, Naoko,Nikaido, Fumi,Yamashita, Masayuki,Ohta, Shunsaku

, p. 4377 - 4380 (2007/10/03)

Diels-Alder-type dimerization of various 5-ethenyl-2-phenylsulfanyl-1H-imidazoles provided a novel highly regio- and stereoselective route to the preparation of multifunctionalized 4,5,6,7-tetrahydrobenzimidazoles, the basic skeleton of ageliferin, a biol

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