Welcome to LookChem.com Sign In|Join Free
  • or
4-(4-[(2-chloroethyl)carbamoyl]aminophenyl)butanoic acid is a complex organic compound belonging to the phenylalkylamine class. It features a butanoic acid backbone with a phenyl group at the fourth position, a carbamoyl amino group at the same position on the phenyl ring, and a 2-chloroethyl group attached to the carbamoyl amino group. This intricate structure suggests a targeted mechanism of action, making it a potential candidate for pharmaceutical applications, particularly as a chemotherapeutic agent.

13908-55-9

Post Buying Request

13908-55-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

13908-55-9 Usage

Uses

Used in Pharmaceutical Industry:
4-(4-[(2-chloroethyl)carbamoyl]aminophenyl)butanoic acid is used as a chemotherapeutic agent for its potential to target specific biological processes within the body. Its complex molecular structure allows for a focused approach to treating certain medical conditions, particularly those requiring intervention at the cellular level.
Used in Cancer Treatment:
In the field of oncology, 4-(4-[(2-chloroethyl)carbamoyl]aminophenyl)butanoic acid is utilized as an anticancer drug. Its unique structure may enable it to interact with specific cellular targets, thereby inhibiting the growth and proliferation of cancer cells. This targeted action could lead to more effective treatments with fewer side effects compared to traditional chemotherapy.
Used in Drug Development Research:
4-(4-[(2-chloroethyl)carbamoyl]aminophenyl)butanoic acid serves as a valuable compound in drug development research. Its specific interactions with biological systems can provide insights into the development of new pharmaceuticals with improved efficacy and selectivity. Researchers can study its mechanism of action to design drugs that are more effective against particular diseases or conditions.
Used in Targeted Drug Delivery Systems:
4-(4-[(2-chloroethyl)carbamoyl]aminophenyl)butanoic acid's unique structure also makes it a candidate for use in targeted drug delivery systems. By attaching therapeutic agents to 4-(4-[(2-chloroethyl)carbamoyl]aminophenyl)butanoic acid or its derivatives, it may be possible to enhance the delivery of drugs to specific cells or tissues, improving treatment outcomes and reducing side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 13908-55-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,0 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13908-55:
(7*1)+(6*3)+(5*9)+(4*0)+(3*8)+(2*5)+(1*5)=109
109 % 10 = 9
So 13908-55-9 is a valid CAS Registry Number.

13908-55-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[4-(2-chloroethylcarbamoylamino)phenyl]butanoic acid

1.2 Other means of identification

Product number -
Other names 4-(4-{[(2-chloroethyl)carbamoyl]amino}phenyl)butanoic acid

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:13908-55-9 SDS

13908-55-9Downstream Products

13908-55-9Relevant academic research and scientific papers

1-Aryl-3-(2-chloroethyl) ureas: Synthesis and in vitro assay as potential anticancer agents

Gaudreault,lacroix,Page,Joly

, p. 185 - 187 (2007/10/02)

1-Aryl-3-(2-chlorethyl) ureas and 1-aryl-3-nitrose-3-(2-chloroethyl) ureas, derived from 4-phenylbutyric acid and alkylanillines, were synthesized and their cytotoxicity was evaluated on human adenocarcinoma cells in vitro. Methyl 4-[p-[3-(2-chloroethyl)ureido]-phenyl]butyrate, 4-methyl [3-(2-chloroethyl)ureido]benzene, and 4-butyl[3-(2-chloroethyl)ureido]benzene were found to be at least as cytotoxic as 4-[p-[bis-(2-chloroethyl)amino]phenyl]butyric acid (chlorambucil), while their N-nitrose derivatives were inactive.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 13908-55-9