13732-32-6 Usage
Uses
Used in Chemical Analysis:
2,3-Butanedione mono(phenylhydrazone) is used as a reagent for detecting and quantifying carbonyl compounds due to its high sensitivity to light, which allows for accurate photometric measurements.
Used in Organic Synthesis:
2,3-BUTANEDIONEMONO(PHENYLHYDRAZONE) is employed in the synthesis of various organic compounds, contributing to the development of new chemical entities and materials.
Used in Pharmaceutical Research:
2,3-Butanedione mono(phenylhydrazone) has potential applications in pharmaceutical research, where it may be utilized in the development of new drugs or as an intermediate in complex organic synthesis processes.
Used in Industrial Processes:
It is also used in industrial processes, where its properties can be harnessed for specific applications, such as in the production of specialty chemicals or materials.
Check Digit Verification of cas no
The CAS Registry Mumber 13732-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,3 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13732-32:
(7*1)+(6*3)+(5*7)+(4*3)+(3*2)+(2*3)+(1*2)=86
86 % 10 = 6
So 13732-32-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O/c1-8(9(2)13)11-12-10-6-4-3-5-7-10/h3-7,12H,1-2H3
13732-32-6Relevant academic research and scientific papers
Synthesis of 2-Substituted 1,2,3-Triazoles via an Intramolecular N–N Bond Formation
Chen, Cheng-yi,Lu, Xiaowei,Holland, Mareike C.,Lv, Shichang,Ji, Xuebao,Liu, Wei,Liu, Jie,Depre, Dominique,Westerduin, Pieter
supporting information, p. 548 - 551 (2019/12/24)
An efficient synthesis of 2-aryl 1,2,3-triazoles based on an intramolecular N–N bond formation is described. Selective activation of bis-hydrazone at the dimethylamino hydrazone group with MeI forms a mono-hydrazonium species. Treatment of the hydrazonium
Addition of Semidione Radicals to Arenediazonium Ions: Synthesis of 1,1-Diacyl-2-arylhydrazines
Clerici, Angelo,Porta, Ombretta
, p. 6813 - 6818 (2007/10/02)
The α-dicarbonyl compounds 1 are selectively reduced to semidione radicals 2 by aqueous Ti3+, via inner-sphere electron transfer (ET).When an equimolar amount of an arenediazonium salt (3) is present, 2 adds to the nitrogen-nitrogen triple bond of 3 to afford the intermediate azo radical cation C, which, depending on the nature of the para substituent of the N-phenyl ring, undergoes rearrangement to a 1,1-diacyl-2-arylhydrazine (4) or preferentially reduction to a hydrazone (5).A mechanism that accounts for both the rearrangement and the substituent effects that are observed is proposed.
