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121106-06-7

5-t-butylthio-3-methoxy-6-phenylpyridazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 121106-06-7 Structure

  • Basic information

    1. Product Name: 5-t-butylthio-3-methoxy-6-phenylpyridazine
    2. Synonyms:
    3. CAS NO:121106-06-7
    4. Molecular Formula:
    5. Molecular Weight: 274.387
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121106-06-7.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: 5-t-butylthio-3-methoxy-6-phenylpyridazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-t-butylthio-3-methoxy-6-phenylpyridazine(121106-06-7)
    11. EPA Substance Registry System: 5-t-butylthio-3-methoxy-6-phenylpyridazine(121106-06-7)

  • 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: 121106-06-7(Hazardous Substances Data)

121106-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121106-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,1,0 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 121106-06:
(8*1)+(7*2)+(6*1)+(5*1)+(4*0)+(3*6)+(2*0)+(1*6)=57
57 % 10 = 7
So 121106-06-7 is a valid CAS Registry Number.

121106-06-7Relevant articles and documents

Pyridazines with Heteroatom Substituents in Position 3 and 5. 2 . Regioselective Introduction of Mercapto Groups in Pyridazines

Olesen, Preben H.,Kappe, Thomas

, p. 1719 - 1723 (2007/10/02)

The nucleophilic substitution of halogen in 3,5-dichloro-6-phenylpyridazine 1, 5-chloro-2-methyl-6-phenylpyridazin-3(2H)-one 13 as well as in 3-chloro-2-methyl-6-phenylpyridazin-5(2H)-one 14 with methoxy, ethoxy, and the 2-methyl-2-propanethiolate anion is described.In the last type of compounds the t-butylthio groups can be eliminated regioselectively with Lewis acids, resulting in the formation of monomercapto and monothiopyridazines.

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