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CAS

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438219-37-5

4-(4-ISOBUTYLPHENYL)-5-METHYL-1,3-THIAZOL-2-AMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 438219-37-5 Structure

  • Basic information

    1. Product Name: 4-(4-ISOBUTYLPHENYL)-5-METHYL-1,3-THIAZOL-2-AMINE
    2. Synonyms: 4-(4-ISOBUTYLPHENYL)-5-METHYL-1,3-THIAZOL-2-AMINE;[4-(4-isobutylphenyl)-5-methyl-thiazol-2-yl]amine;4-(4-isobutylphenyl)-5-methyl-2-thiazolamine;4-(4-isobutylphenyl)-5-methyl-thiazol-2-amine;5-methyl-4-[4-(2-methylpropyl)phenyl]-1,3-thiazol-2-amine;IVK/1011839;Oprea1_098924;ZINC00373353
    3. CAS NO:438219-37-5
    4. Molecular Formula: C14H18N2S
    5. Molecular Weight: 246.37112
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 438219-37-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(4-ISOBUTYLPHENYL)-5-METHYL-1,3-THIAZOL-2-AMINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-ISOBUTYLPHENYL)-5-METHYL-1,3-THIAZOL-2-AMINE(438219-37-5)
    11. EPA Substance Registry System: 4-(4-ISOBUTYLPHENYL)-5-METHYL-1,3-THIAZOL-2-AMINE(438219-37-5)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 438219-37-5(Hazardous Substances Data)

438219-37-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 438219-37-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,8,2,1 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 438219-37:
(8*4)+(7*3)+(6*8)+(5*2)+(4*1)+(3*9)+(2*3)+(1*7)=155
155 % 10 = 5
So 438219-37-5 is a valid CAS Registry Number.

438219-37-5Downstream Products

438219-37-5Relevant articles and documents

Iridium-catalyzed 1,3-hydrogen shift/chlorination of allylic alcohols

Ahlsten, Nanna,Gomez, Antonio Bermejo,Martin-Matute, Belen

, p. 6273 - 6276 (2013/07/05)

Tandem: Allylic alcohols react with N-chlorosuccinimide (NCS) in a tandem 1,3-H shift/C-Cl bond formation leading to α-chloroketones and α-chloroaldehydes. The reactions proceed with complete selectivity to give single constitutional isomers of monochlorinated carbonyl compounds. The utility of the transformation is illustrated by the straightforward synthesis of 4,5-disubstituted 2-aminothiazoles from allylic alcohols. Copyright

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