7539-24-4 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
1,3-Benzenediol, 4-nitro-, 1-benzoate is derived from 1,3-benzenediol, which is a type of phenol.
Explanation
The compound has a 4-nitro group (-NO2) attached to the benzene ring and a benzoate group (-COO-) attached to the hydroxyl group of 1,3-benzenediol.
Explanation
The compound is used in various industries, including the production of pharmaceuticals, as a reagent in organic synthesis, and has potential applications in medicinal chemistry due to its ability to modulate biochemical processes.
5. Potential toxicity and hazardous nature
Explanation
1,3-Benzenediol, 4-nitro-, 1-benzoate should be handled with care and proper safety precautions due to its potential toxic and hazardous properties.
Explanation
When working with 1,3-Benzenediol, 4-nitro-, 1-benzoate, it is essential to follow safety guidelines and use appropriate protective equipment to minimize the risk of exposure and potential harm.
Derivative of
1,3-Benzenediol
Functional groups
4-nitro group and benzoate group
Applications
Pharmaceutical production, organic synthesis, and medicinal chemistry
Safety measures
Proper handling and safety precautions
Check Digit Verification of cas no
The CAS Registry Mumber 7539-24-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,3 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7539-24:
(6*7)+(5*5)+(4*3)+(3*9)+(2*2)+(1*4)=114
114 % 10 = 4
So 7539-24-4 is a valid CAS Registry Number.
7539-24-4Relevant academic research and scientific papers
Ji, Xiujie,Li, Chunbao
, p. 2478 - 2482 (2006)
Nitro-substituted phenolic esters and sulfonates were successfully and selectively deacylated and desulfonated, respectively. The directing effect of the nitro group is supported by the excellent regioselectivities and good yields. These reactions demonst
Potential Hypolipidemic Agents: Part IV - Synthesis and Hypolipidemic Activities of Some New Ethyl 3-Aryl-2H-1,4-benzoxazin-7-yloxyalkanoates
Shridhar, D. R.,Ram, Bhagat,Reddy, G. Jagath
, p. 883 - 885 (2007/10/02)
A number of ethyl 3-aryl-2H-1,4-benzoxazin-7-yloxyalkanoates have been synthesised by O-alkylation of the corresponding 7-hydroxy-3-aryl-2H-1,4-benzoxazines (Va-c) and evaluated for their hypolipidemic activity in rats.
