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CAS

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346725-77-7

4-tert-butyl-N-(3,5-dimethylphenyl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 346725-77-7 Structure

  • Basic information

    1. Product Name: 4-tert-butyl-N-(3,5-dimethylphenyl)benzamide
    2. Synonyms: 4-tert-butyl-N-(3,5-dimethylphenyl)benzamide
    3. CAS NO:346725-77-7
    4. Molecular Formula: C19H23NO
    5. Molecular Weight: 281.39202
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 346725-77-7.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-tert-butyl-N-(3,5-dimethylphenyl)benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-tert-butyl-N-(3,5-dimethylphenyl)benzamide(346725-77-7)
    11. EPA Substance Registry System: 4-tert-butyl-N-(3,5-dimethylphenyl)benzamide(346725-77-7)

  • 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: 346725-77-7(Hazardous Substances Data)

346725-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 346725-77-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,6,7,2 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 346725-77:
(8*3)+(7*4)+(6*6)+(5*7)+(4*2)+(3*5)+(2*7)+(1*7)=167
167 % 10 = 7
So 346725-77-7 is a valid CAS Registry Number.

346725-77-7Downstream Products

346725-77-7Relevant articles and documents

Direct Amidation of N-Boc- and N-Cbz-Protected Amines via Rhodium-Catalyzed Coupling of Arylboroxines and Carbamates

Lim, Diane S. W.,Lew, Tedrick T. S.,Zhang, Yugen

, p. 6054 - 6057 (2016/01/09)

N-Boc- and N-Cbz-protected amines are directly converted into amides by a novel rhodium-catalyzed coupling of arylboroxines and carbamates, replacing the traditional two-step deprotection-condensation sequence. Both protected anilines and aliphatic amines are efficiently transformed into a wide variety of secondary benzamides, including sterically hindered and electron-deficient amides, as well as in the presence of acid-labile and reducible functional groups.

Copper(i)-catalyzed amidation reaction of organoboronic esters and isocyanates

Salim Lew, Tedrick Thomas,Wen Lim, Diane Shu,Zhang, Yugen

, p. 5140 - 5143 (2015/12/05)

A simple and efficient methodology for the preparation of amides from easily available organoboronic esters and isocyanates has been accomplished using a ligand-free copper(i) catalyst. The reaction system demonstrated a broad substrate scope and provided convenient access to a wide variety of secondary amides.

Pharmaceutical compositions containing phenylamides

-

, (2008/06/13)

Pharmaceutical compositions for inhibiting the aggregation of erthyrocytes or thrombocytes which include phenylamides which conform to the formula: STR1 with R1-6, X, A and B being as defined. Processes for the preparation of novel phenylamides

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