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67319-05-5

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

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  • 67319-05-5 Structure

  • Basic information

    1. Product Name: 1H-Imidazole, 1-(methoxymethyl)-2-(phenylthio)-
    2. Synonyms:
    3. CAS NO:67319-05-5
    4. Molecular Formula: C11H12N2OS
    5. Molecular Weight: 220.295
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 67319-05-5.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: 1H-Imidazole, 1-(methoxymethyl)-2-(phenylthio)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Imidazole, 1-(methoxymethyl)-2-(phenylthio)-(67319-05-5)
    11. EPA Substance Registry System: 1H-Imidazole, 1-(methoxymethyl)-2-(phenylthio)-(67319-05-5)

  • 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: 67319-05-5(Hazardous Substances Data)

67319-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67319-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,1 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67319-05:
(7*6)+(6*7)+(5*3)+(4*1)+(3*9)+(2*0)+(1*5)=135
135 % 10 = 5
So 67319-05-5 is a valid CAS Registry Number.

67319-05-5Relevant articles and documents

Synthetic studies on dragmacidin D: Synthesis and assembly of three fragments towards an advanced intermediate

Oikawa, Masato,Ikoma, Minoru,Sasaki, Makoto

experimental part, p. 4654 - 4666 (2011/10/03)

We report herein the approach to the key advanced intermediate in the synthesis of the bioactive marine natural product dragmacidin D. By employing a modular synthesis strategy of three fragments (5, 7, and 8), the advanced intermediate 3 has been successfully synthesized in 2.5% yield over 15 steps by starting from nitrotoluene 20. The synthesis also involves sequential cross-coupling reactions, namely Sonogashira and Suzuki-Miyaura reactions, so that various analogues can be efficiently synthesized, which will allow the study of structure-activity relationships of dragmacidin D.

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

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

experimental part, 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

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