3590-12-3 Usage
Description
(Phenylimino)diethane-2,1-diyl bis(4-methylbenzenesulfonate) is a chemical compound characterized by its molecular formula C26H28N2O10S2. It is a sulfonate ester derived from phenylimine and diethane-2,1-diyl bis(4-methylbenzenesulfonate), known for its applications in organic synthesis and as a reactive intermediate in the production of pharmaceuticals and agrochemicals. (phenylimino)diethane-2,1-diyl bis(4-methylbenzenesulfonate) also serves as a reagent in chemical reactions, particularly in the formation of carbon-carbon bonds. However, it is essential to handle and store this chemical with care due to its potentially hazardous properties, such as being harmful if swallowed or inhaled.
Uses
Used in Organic Synthesis:
(Phenylimino)diethane-2,1-diyl bis(4-methylbenzenesulfonate) is used as a key component in organic synthesis for the creation of various chemical compounds. Its unique structure allows it to participate in a range of reactions, making it a valuable asset in the field of chemistry.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (phenylimino)diethane-2,1-diyl bis(4-methylbenzenesulfonate) is utilized as a reactive intermediate. Its role in the synthesis of specific drugs contributes to the development of new medications and therapies.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, (phenylimino)diethane-2,1-diyl bis(4-methylbenzenesulfonate) is employed as an intermediate in the production of various agrochemicals, such as pesticides and fertilizers, which are essential for agricultural productivity.
Used as a Reagent in Chemical Reactions:
(Phenylimino)diethane-2,1-diyl bis(4-methylbenzenesulfonate) is also used as a reagent in chemical reactions, particularly those involving the formation of carbon-carbon bonds. Its participation in these reactions aids in the synthesis of complex organic molecules.
Safety Precautions:
Due to its potentially hazardous properties, it is crucial to handle and store (phenylimino)diethane-2,1-diyl bis(4-methylbenzenesulfonate) with caution and in accordance with safety guidelines. This includes using appropriate personal protective equipment (PPE) and ensuring proper ventilation during its use.
Check Digit Verification of cas no
The CAS Registry Mumber 3590-12-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,9 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3590-12:
(6*3)+(5*5)+(4*9)+(3*0)+(2*1)+(1*2)=83
83 % 10 = 3
So 3590-12-3 is a valid CAS Registry Number.
3590-12-3Relevant articles and documents
Selective Detection of Cu+ Ions in Live Cells via Fluorescence Lifetime Imaging Microscopy
Kuimova, Marina K.,Lewis, Benjamin W.,Priessner, Martin,Sastre, Magdalena,Summers, Peter A.,Vilar, Ramon,Ying, Liming
supporting information, p. 23148 - 23153 (2021/09/20)
Copper is an essential trace element in living organisms with its levels and localisation being carefully managed by the cellular machinery. However, if misregulated, deficiency or excess of copper ions can lead to several diseases. Therefore, it is impor
Redox triggered aggregation induced emission (AIE) polymers with azobenzene pendants
Wu, Bing,Wang, Wei,Wang, Jilei,Li, Shang,He, Yaning
, p. 290 - 297 (2018/05/24)
We reported the redox triggered aggregation induced emission (AIE) polymers with azobenzene pendants. Tetraphenylethene (TPE) based polymers with selected degrees of functionalization of azobenzene chromophores were synthesized through a post-polymerizati
Synthesis of New Bis-1,2,4-Oxadiazoline Derivatives via 1,3-Dipolar Cycloaddition Reaction
Chen, Fei,Zeng, Hua,Liu, Fang-Ming
, p. 1866 - 1870 (2016/11/23)
A series of novel bis-oxadiazoline derivatives 4 was synthesized via 1,3-dipolar cycloaddition reaction of bis-aldimines 3, and nitrile oxides generated in situ from various benzohydroximinoyl chlorides in the presence of Et3N. The target products were confirmed by IR,1H-NMR, and mass spectrometry.
