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7539-24-4

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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 this compound, 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 articles and documents

Nitro-group-directed selective deacylation and desulfonation

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

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