77601-83-3 Usage
Uses
Used in Organic Synthesis:
(2,4,6-trinitrophenyl)acetic acid is used as a reagent in organic synthesis for the preparation of various chemical compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the synthesis of new molecules.
Used in Research:
In the field of research, (2,4,6-trinitrophenyl)acetic acid is utilized as a tool to study chemical reactions and mechanisms. Its properties and reactivity provide insights into the behavior of similar compounds and contribute to the advancement of chemical knowledge.
Used in Dye Production:
(2,4,6-trinitrophenyl)acetic acid is used as a starting material in the production of dyes. Its ability to impart color makes it a useful component in the creation of various dyes for different industries.
Used in Explosive Manufacturing:
Due to its highly explosive nature, (2,4,6-trinitrophenyl)acetic acid is used in the manufacturing of explosives. Its properties make it a potent component in the production of certain types of explosives.
Used in Chemical Analysis:
(2,4,6-trinitrophenyl)acetic acid is employed as a reagent in chemical analysis to detect and quantify the presence of specific substances. Its reactivity and color-changing properties make it a useful indicator in various analytical techniques.
Used in Safety and Precaution:
Given its highly explosive nature, (2,4,6-trinitrophenyl)acetic acid is a critical component in the development of safety protocols and precautions for handling and storage. Understanding its properties and potential hazards is essential for ensuring the safe use of (2,4,6-trinitrophenyl)acetic acid in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 77601-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,0 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77601-83:
(7*7)+(6*7)+(5*6)+(4*0)+(3*1)+(2*8)+(1*3)=143
143 % 10 = 3
So 77601-83-3 is a valid CAS Registry Number.
77601-83-3Relevant academic research and scientific papers
Synthesis of 1-aryl-4,6-dinitro-1H-indazoyl-3-methylcarboxylates
Rozhkov,Vorob'ov,Lobatch,Kuvshinov,Shevelev
, p. 467 - 472 (2007/10/03)
Synthesis of 1-aryl-4,6-dinitro-1H-indazoyl-3-methylcarboxylates from 2,4,6-trinitrotoluene derivatives is reported.
Synthetic utilization of polynitroaromatic compounds. 1. S-derivatization of 1-substituted 2,4,6-trinitrobenzenes with thiols
Zlotin,Kislitsin,Samet,Serebryakov,Konyushkin,Semenov,Buchanan III,Gakh
, p. 8430 - 8438 (2007/10/03)
Reactions of 1-R-2,4,6-trinitrobenenes (R = alkyl, protected aldehyde, aminocarbonyl, cyano groups, or isoxazole ring) with thiol salts were investigated. In most cases, these reactions gave a mixture of minor para and major ortho substitution products. Reactions of N,N-disubstituted 2,4,6-trinitrobenzamides with S-,O-, and N-nucleophiles afforded products of substitution of the p-nitro group exclusively. 1-Cyano-2,4,6-trinitrobenzene was found to be the most reactive and the least selective: all three nitro groups can be substituted using an excess of thiol salts. 2-R-4,6-dinitrobenzamides showed no regioselectivity under similar conditions to yield 1:1 mixtures of para and ortho isomers.
Process for the production of esters exhibiting nonlinear optical response
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, (2008/06/13)
This invention provides multistep process embodiments for the production of novel esters which exhibit nonlinear optical response. A process embodiment is illustrated by the reaction of a Schiff base with a substituted acetic acid to form a stilbene alcohol intermediate: STR1 The stilbene alcohol intermediate is decarboxylated, and then is esterified in the presence of a pyridine type catalyst to provide an ester with a conjugated structure.
