Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1429-24-9

Ethyl 4-({[4-(ethoxycarbonyl)phenyl]carbamothioyl}amino)benzoate is a complex organic compound with the chemical formula C19H18N2O4S. It is a derivative of benzoic acid, featuring a carbamoylthio group attached to the 4-position of the benzene ring. The molecule also contains an ethyl ester group at the 4-position of another benzene ring, which is connected to the main structure through an amide linkage. ethyl 4-({[4-(ethoxycarbonyl)phenyl]carbamothioyl}amino)benzoate is characterized by its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of various chemical compounds. Its structure provides a platform for further functionalization and modification, making it a valuable building block in organic chemistry.

1429-24-9 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1429-24-9 Structure

  • Basic information

    1. Product Name: ethyl 4-({[4-(ethoxycarbonyl)phenyl]carbamothioyl}amino)benzoate
    2. Synonyms: benzoic acid, 4,4'-(carbonothioyldiimino)bis-, diethyl ester; Ethyl 4-({[4-(ethoxycarbonyl)phenyl]carbamothioyl}amino)benzoate
    3. CAS NO:1429-24-9
    4. Molecular Formula: C19H20N2O4S
    5. Molecular Weight: 372.4381
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1429-24-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 504.1°C at 760 mmHg
    3. Flash Point: 258.7°C
    4. Appearance: N/A
    5. Density: 1.299g/cm3
    6. Vapor Pressure: 2.73E-10mmHg at 25°C
    7. Refractive Index: 1.655
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: ethyl 4-({[4-(ethoxycarbonyl)phenyl]carbamothioyl}amino)benzoate(CAS DataBase Reference)
    11. NIST Chemistry Reference: ethyl 4-({[4-(ethoxycarbonyl)phenyl]carbamothioyl}amino)benzoate(1429-24-9)
    12. EPA Substance Registry System: ethyl 4-({[4-(ethoxycarbonyl)phenyl]carbamothioyl}amino)benzoate(1429-24-9)

  • 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: 1429-24-9(Hazardous Substances Data)

1429-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1429-24-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1429-24:
(6*1)+(5*4)+(4*2)+(3*9)+(2*2)+(1*4)=69
69 % 10 = 9
So 1429-24-9 is a valid CAS Registry Number.

1429-24-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-[(4-ethoxycarbonylphenyl)carbamothioylamino]benzoate

1.2 Other means of identification

Product number -
Other names 4,4'-Thioureylen-di-benzoesaeure-diaethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1429-24-9 SDS

1429-24-9Relevant articles and documents

Synthesis, characterization, and pharmacological evaluation of thiourea derivatives

Alghamdi, Saad,Naz, Sumaira,Sahibzada, Muhammad Umar Khayam,Ulbari, Wasim,Umar, Muhammad Naveed,Zahoor, Muhammad

, p. 764 - 777 (2020/07/20)

Thioureas and their derivatives are organosulfur compounds having applications in numerous fields such as organic synthesis and pharmaceutical industries. Symmetric thiourea derivatives were synthesized by the reaction of various anilines with CS2. The synthesized compounds were characterized using the UV-visible and nuclear magnetic resonance (NMR) spectroscopic techniques. The compounds were screened for in vitro inhibition of α-amylase, α-glucosidase, acetylcholinesterase (AChE), and butyrylcholinesterase (BuChE) enzymes and for their antibacterial and antioxidant potentials. These compounds were fed to Swiss male albino mice to evaluate their toxicological effects and potential to inhibit glucose-6-phosphatase (G6Pase) inhibition. The antibacterial studies revealed that compound 4 was more active against the selected bacterial strains. Compound 1 was more active against 2,2-diphenyl-1-picrylhydrazyl and 2,2'-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) free radicals, AChE, BuChE, and α-glucosidase. Compound 2 was more potent against α-amylase and G6Pase. Toxicity studies showed that compound 4 is safe as it exerted no toxic effect on any of the hematological and biochemical parameters or on liver histology of the experimental animals at any studied dose rate. The synthesized compounds showed promising antibacterial and antioxidant potential and were very active (both in vitro and in vivo) against G6Pase and moderately active against the other selected enzymes used in this study.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1429-24-9