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4-(benzyloxy)-N,N-dimethylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 84403-55-4 Structure
  • Basic information

    1. Product Name: 4-(benzyloxy)-N,N-dimethylbenzamide
    2. Synonyms: 4-(benzyloxy)-N,N-dimethylbenzamide
    3. CAS NO:84403-55-4
    4. Molecular Formula:
    5. Molecular Weight: 255.316
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 84403-55-4.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: 4-(benzyloxy)-N,N-dimethylbenzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(benzyloxy)-N,N-dimethylbenzamide(84403-55-4)
    11. EPA Substance Registry System: 4-(benzyloxy)-N,N-dimethylbenzamide(84403-55-4)
  • 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: 84403-55-4(Hazardous Substances Data)

84403-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84403-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,0 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84403-55:
(7*8)+(6*4)+(5*4)+(4*0)+(3*3)+(2*5)+(1*5)=124
124 % 10 = 4
So 84403-55-4 is a valid CAS Registry Number.

84403-55-4Relevant articles and documents

A mild and practical method for deprotection of aryl methyl/benzyl/allyl ethers with HPPh2andtBuOK

Pan, Wenjing,Li, Chenchen,Zhu, Haoyin,Li, Fangfang,Li, Tao,Zhao, Wanxiang

supporting information, p. 7633 - 7640 (2021/09/22)

A general method for the demethylation, debenzylation, and deallylation of aryl ethers using HPPh2andtBuOK is reported. The reaction features mild and metal-free reaction conditions, broad substrate scope, good functional group compatibility, and high chemical selectivity towards aryl ethers over aliphatic structures. Notably, this approach is competent to selectively deprotect the allyl or benzyl group, making it a general and practical method in organic synthesis.

INHIBITORS OF HIV REPLICATION

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Page/Page column 42, (2010/11/03)

Compounds of formula (I): wherein R1, R2, A1, A2, A3, A4, X and Y are as defined herein, are useful as inhibitors of HIV replication.

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