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2300-16-5

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2300-16-5 Usage

General Description

3,6-dinitrophthalic acid is a chemical compound that is derived from phthalic acid and is a dinitro derivative. It is a yellow crystalline solid with moderate solubility in water. It is primarily used as a building block in the synthesis of various organic compounds, such as dyes, pigments, and polymers. 3,6-dinitrophthalic acid is also known for its use as a corrosion inhibitor in the oil and gas industry. In addition, it has been utilized as a reagent in the analysis of amino acids and proteins. However, it is important to note that 3,6-dinitrophthalic acid is considered hazardous and should be handled with proper safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 2300-16-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,0 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2300-16:
(6*2)+(5*3)+(4*0)+(3*0)+(2*1)+(1*6)=35
35 % 10 = 5
So 2300-16-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H4N2O8/c11-7(12)5-3(9(15)16)1-2-4(10(17)18)6(5)8(13)14/h1-2H,(H,11,12)(H,13,14)

2300-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-dinitrophthalic acid

1.2 Other means of identification

Product number -
Other names 3,6-dinitrobenzene-1,2-dioic 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:2300-16-5 SDS

2300-16-5Relevant articles and documents

Overcoming regioselectivity issues inherent in bis-Troeger's base preparation

Havlik, Martin,Kral, Vladimir,Dolensky, Bohumil

, p. 4867 - 4870 (2007/10/03)

(Figure Presented) Bis-Troeger's base derivatives are a new family of molecular tweezers. A major drawback to their study is a lack of commercially available precursors, ortho-nitrocarboxylic acids. A reverse synthetic strategy starting from known dinitrodicarboxylic acids, which circumvents this problem, is presented. Via this methodology regioisomeric bis-TB derivatives can be prepared selectively, using only common aromatic amines that are typically commercially available.

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