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(BUTYLAMINO)-N-(3-METHOXYPHENYL)FORMAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 195133-27-8 Structure
  • Basic information

    1. Product Name: (BUTYLAMINO)-N-(3-METHOXYPHENYL)FORMAMIDE
    2. Synonyms: (BUTYLAMINO)-N-(3-METHOXYPHENYL)FORMAMIDE;1-(M-ANISYL)-3-BUTYLUREA;3-butyl-1-(3-methoxyphenyl)urea
    3. CAS NO:195133-27-8
    4. Molecular Formula: C12H18N2O2
    5. Molecular Weight: 222.28
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 195133-27-8.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: (BUTYLAMINO)-N-(3-METHOXYPHENYL)FORMAMIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: (BUTYLAMINO)-N-(3-METHOXYPHENYL)FORMAMIDE(195133-27-8)
    11. EPA Substance Registry System: (BUTYLAMINO)-N-(3-METHOXYPHENYL)FORMAMIDE(195133-27-8)
  • 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: 195133-27-8(Hazardous Substances Data)

195133-27-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 195133-27-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,1,3 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 195133-27:
(8*1)+(7*9)+(6*5)+(5*1)+(4*3)+(3*3)+(2*2)+(1*7)=138
138 % 10 = 8
So 195133-27-8 is a valid CAS Registry Number.

195133-27-8Downstream Products

195133-27-8Relevant articles and documents

Copper-catalyzed formation of carbon-heteroatom and carbon-carbon bonds

-

, (2015/03/06)

The present invention relates to copper-catalyzed carbon-heteroatom and carbon-carbon bond-forming methods. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of an amide or amine moiety and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In additional embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between a nitrogen atom of an acyl hydrazine and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In other embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of a nitrogen-containing heteroaromatic, e.g., indole, pyrazole, and indazole, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-oxygen bond between the oxygen atom of an alcohol and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. The present invention also relates to copper-catalyzed methods of forming a carbon-carbon bond between a reactant comprising a nucleophilic carbon atom, e.g., an enolate or malonate anion, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. Importantly, all the methods of the present invention are relatively inexpensive to practice due to the low cost of the copper comprised by the catalysts.

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