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4-(Allylamino)benzoic acid, with the molecular formula C10H11NO2, is a benzoic acid derivative featuring an allylamine group attached to the fourth position of the benzene ring. 4-(ALLYLAMINO)BENZOIC ACID serves as a valuable building block in medicinal and synthetic chemistry due to its unique structure and functional groups.

53624-18-3

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53624-18-3 Usage

Uses

Used in Pharmaceutical Synthesis:
4-(Allylamino)benzoic acid is utilized as a key intermediate in the synthesis of pharmaceutical drugs and other organic compounds. Its presence in the molecular structure allows for the development of new therapeutic agents with potential applications in various medical fields.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-(Allylamino)benzoic acid is used as a versatile building block for the creation of a variety of organic molecules. Its unique structure and functional groups enable the design and synthesis of new compounds with potential therapeutic properties.
Used in Anti-inflammatory and Analgesic Applications:
4-(Allylamino)benzoic acid has been studied for its potential as an anti-inflammatory and analgesic agent. Its allylamine group may contribute to these properties, making it a promising candidate for the development of new medications to treat pain and inflammation.

Check Digit Verification of cas no

The CAS Registry Mumber 53624-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,2 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53624-18:
(7*5)+(6*3)+(5*6)+(4*2)+(3*4)+(2*1)+(1*8)=113
113 % 10 = 3
So 53624-18-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO2/c1-2-7-11-9-5-3-8(4-6-9)10(12)13/h2-6,11H,1,7H2,(H,12,13)

53624-18-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(prop-2-enylamino)benzoic acid

1.2 Other means of identification

Product number -
Other names F3095-3188

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:53624-18-3 SDS

53624-18-3Relevant academic research and scientific papers

A new method for the facile synthesis of hydroxylated flavones by using allyl protection

Nawghare,Sakate,Lokhande

, p. 291 - 302 (2014/04/17)

The iodine-induced oxidative cyclization of 2′-hydroxychalcones provides a simple, highly efficient approach to various hydroxy flavones and analogues. This process is run under mild conditions, tolerates various functional groups, and provides hydroxy flavones in good to excellent yield. The allyl-protected acetophenones and benzaldehydes were smoothly deallylated under similar conditions.

TREATMENT OF CANCER USING THE SODIUM SALT OF A BENZOIC ACID DERIVATIVE

-

Page/Page column 25, (2011/04/18)

The present invention provides a method of treating cancer using the sodium salt of a benzoic acid derivative, alone or in combination with standard treatments such as chemotherapy and radiotherapy.

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