77601-83-3 Usage
Description
(2,4,6-trinitrophenyl)acetic acid, also known as picrylacetic acid, is a chemical compound with the molecular formula C8H5N3O8. It is a derivative of trinitrophenol and is characterized by its yellow to brownish-colored appearance. (2,4,6-trinitrophenyl)acetic acid is known for its use in various applications due to its unique properties, despite being highly explosive and requiring careful handling and storage.
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 this compound 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 articles and documents
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.
Process for the production of esters exhibiting nonlinear optical response
-
, (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.
