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3-Benzoyl-4-nitroresorcinol is an organic compound with the chemical formula C13H7NO5. It is a derivative of resorcinol, featuring a nitro group at the 4-position and a benzoyl group at the 3-position. This yellow crystalline solid is used as a chemical intermediate in the synthesis of various pharmaceuticals and dyes. It is also known for its analytical applications, particularly in the determination of halide ions in solution. The compound is sensitive to light and heat, and it is typically stored in a cool, dark place to maintain its stability. Its chemical properties and reactivity make it a valuable component in the development of new chemical entities and analytical methods.

7539-18-6

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7539-18-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7539-18-6 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, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7539-18:
(6*7)+(5*5)+(4*3)+(3*9)+(2*1)+(1*8)=116
116 % 10 = 6
So 7539-18-6 is a valid CAS Registry Number.

7539-18-6SDS

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 5-hydroxy-2-nitrophenyl benzoate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:7539-18-6 SDS

7539-18-6Relevant academic research and scientific papers

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.

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