13732-32-6 Usage
Description
2,3-Butanedione mono(phenylhydrazone), with the molecular formula C10H14N2O, is a chemical compound derived from 2,3-butanedione. It is known for its yellow to orange solid form and high sensitivity to light, which makes it suitable for photometric measurements. 2,3-BUTANEDIONEMONO(PHENYLHYDRAZONE) is commonly utilized in chemical analysis as a reagent for detecting and quantifying carbonyl compounds. Additionally, it finds applications in the synthesis of various organic compounds and holds potential in pharmaceutical research and industrial processes. Due to its potential harmful effects if ingested, inhaled, or causing skin and eye irritation, careful handling is advised.
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 articles and documents
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
