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303755-59-1

4-(phenylamino)phenyl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 303755-59-1 Structure

  • Basic information

    1. Product Name: 4-(phenylamino)phenyl benzoate
    2. Synonyms: 4-(phenylamino)phenyl benzoate
    3. CAS NO:303755-59-1
    4. Molecular Formula:
    5. Molecular Weight: 289.334
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 303755-59-1.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-(phenylamino)phenyl benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(phenylamino)phenyl benzoate(303755-59-1)
    11. EPA Substance Registry System: 4-(phenylamino)phenyl benzoate(303755-59-1)

  • 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: 303755-59-1(Hazardous Substances Data)

303755-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 303755-59-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,3,7,5 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 303755-59:
(8*3)+(7*0)+(6*3)+(5*7)+(4*5)+(3*5)+(2*5)+(1*9)=131
131 % 10 = 1
So 303755-59-1 is a valid CAS Registry Number.

303755-59-1Relevant articles and documents

Palladium-catalyzed carbonylation of iminoquinones and aryl iodides to access arylp-amino benzoates

Wang, Siqi,Wu, Xiao-Feng,Yao, Lingyun,Ying, Jun

supporting information, p. 8246 - 8249 (2021/10/12)

A palladium-catalyzed carbonylation of iminoquinones and aryl iodides has been developed for the construction of arylp-amino benzoates. Using benzene-1,3,5-triyl triformate (TFBen) as the CO source, the reaction proceeded well to give various arylp-amino benzoates in good to excellent yields. Additionally, control experiments were conducted to gain more insights into the reaction mechanism.

Facile esterification of alcohols with 2-Acyl-4,5-dichloropyridazin-3(2 H)-ones under Friedel-Crafts conditions

Kim, Bo Ram,Sung, Gi Hyeon,Ryu, Ki Eun,Yoon, Hyo Jae,Lee, Sang-Gyeong,Yoon, Yong-Jin

, p. 1909 - 1915 (2014/08/18)

This paper describes the esterification of aromatic and aliphatic alcohols by using 2-acyl-4,5-dichloropyridazin-3(2H)-ones as an acyl source under Friedel-Crafts conditions. Twelve alcohols were reacted with four 2-acyl-4,5-dichloropyridazin-3(2H)-ones in the presence of AlCl3 in tetrahydrofuran at room temperature to give the corresponding esters in moderate to excellent yields. Thus, 2-acylpyridazin-3(2H)-ones serve as good and atom-economic acyl sources for the esterification of aromatic alcohols under Friedel-Crafts conditions, representing a rapid, practical, and efficient method of esterification. Georg Thieme Verlag Stuttgart. New York.

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