71094-29-6 Usage
Uses
Used in Analytical Chemistry:
CNdh is employed as a reagent for the detection and quantification of aldehydes and ketones. Its high reactivity allows it to interact with various functional groups in organic molecules, making it a valuable tool for identifying and studying these compounds.
Used in Chemical Research:
In the realm of chemical research, CNdh serves as an essential compound for understanding the interactions between different organic molecules. Its ability to react with multiple functional groups aids in the exploration of novel chemical reactions and the development of new synthetic pathways.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, CNdh could potentially be used in the pharmaceutical industry for the synthesis of various drugs, given its reactivity with different functional groups. This application would be based on the need for specific chemical reactions to create pharmaceutical compounds.
Safety Precautions:
It is crucial to handle CNdh with care, as it can pose health risks if not used properly. Adequate safety measures should be taken to minimize any potential hazards associated with its use in chemical analysis and research.
Check Digit Verification of cas no
The CAS Registry Mumber 71094-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,9 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 71094-29:
(7*7)+(6*1)+(5*0)+(4*9)+(3*4)+(2*2)+(1*9)=116
116 % 10 = 6
So 71094-29-6 is a valid CAS Registry Number.
71094-29-6Relevant academic research and scientific papers
E/Z isomerism in monoalkylated derivatives of [Pt2(μ-S) 2(PPH3)4] containing 2,4-dinitrophenylhydrazone substituents
Ujam, Oguejiofo T.,Devoy, Sarah M.,Henderson, William,Wilkins, Alistair L.,Nicholson, Brian K.
experimental part, p. 2782 - 2790 (2012/02/15)
Alkylation of [Pt2(μ-S)2(PPH3) 4] with 2,4-dinitrophenylhydrazone-functionalized alkylating agents XC6H4C{=NNHC6H3(NO2) 2}CH2Br (X = H
Kinetics and Mechanism of Oxidation of Alcohols by Ceric Ammonium Nitrate
Mathur, Dwarka, L.,Agarwal, Anupma,Banerji, Kalyan K.
, p. 519 - 522 (2007/10/02)
The main product of the oxidation of secondary alcohol by ceric ammonium nitrate is the corresponding ketone.The reaction is of first-order with respect to the oxidant but exhibit a Michaelis-Menten type kinetics with respect to the alcohol.The formation constants of the alcohol-CeIV complex and its thermodynamic parameters have been calculated.The rate of decomposition of the complex and the activation parameters have also been evaluated.The rates of decomposition of the complex correlate with Taft's ?* values with a low negative reaction constant.The oxidation induced polymerisation of acrylonitrile.The retardation of rate with increasing acidity has been explained on the formation of kinetically inactive protonated alcohol.The protonated constants for the various alcohol have been calculated.The presence of a small primary kinetic isotope effect, kH/kD = 2.3, confirms that the rate-determining step involves a C-H bond rupture in a non-symmetrical transition state.
