52010-90-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound is derived from benzene by replacing one hydrogen atom with an aldehyde group (-CHO) and another with an oxime group (-C=NOH).
Explanation
The color and physical state of the compound, which is a pale yellow solid at room temperature.
Explanation
The temperature range at which the compound transitions from a solid to a liquid state.
Explanation
The compound is commonly used as a reagent in the synthesis of various organic compounds.
Explanation
It serves as an intermediate in the synthesis of heterocyclic compounds, which are organic compounds containing a ring of atoms with at least one atom being non-carbon.
Explanation
The compound poses potential health risks if it is ingested, inhaled, or comes into contact with the skin, and proper safety measures should be taken when handling it.
Explanation
When working with 1,4-Benzenedicarboxaldehyde, monooxime (9CI), it is essential to follow safety guidelines and use appropriate protective equipment to minimize the risk of exposure.
Chemical structure
Aldehyde derivative of benzene
Appearance
Pale yellow solid
Melting point
110-113°C
Usage
Reagent in organic synthesis
Application
Intermediate in the production of heterocyclic compounds
Safety precautions
Harmful if ingested, inhaled, or comes into contact with the skin
Handling
Use proper safety measures
Check Digit Verification of cas no
The CAS Registry Mumber 52010-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,1 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 52010-90:
(7*5)+(6*2)+(5*0)+(4*1)+(3*0)+(2*9)+(1*0)=69
69 % 10 = 9
So 52010-90-9 is a valid CAS Registry Number.
52010-90-9Relevant articles and documents
Synthesis, the electronic properties and efficient photoinduced electron transfer of new pyrrolidine[60]fullerene- and isoxazoline[60]fullerene-BODIPY dyads: Nitrile oxide cycloaddition under mild conditions using PIFA
Cabrera-Espinoza, Andrea,Insuasty, Braulio,Ortiz, Alejandro
, p. 9061 - 9069 (2017)
Two new BODIPY-C60 dyads, with a pyrrolidine linker (BDP-Pyr) and an isoxazoline linker (BDP-Is) between the two electroactive units, have been synthesized and characterized. Their photophysical and electrochemical properties have been studied
A practical and cost-efficient, one-pot conversion of aldehydes into nitriles mediated by 'activated DMSO'
Augustine, John Kallikat,Bombrun, Agnes,Atta, Rajendra Nath
experimental part, p. 2223 - 2227 (2011/10/31)
Participation of activated DMSO in the one-pot transformation of aldehydes to nitriles has been described by reacting aldehydes with NHHHCl in DMSO in the absence of any added base or catalyst. The method is applicable to access a wide range of aromatic, heterocyclic, and aliphatic nitriles, in which only water is a byproduct. A straightforward and practical procedure is demonstrated on a multigram scale. Georg Thieme Verlag Stuttgart - New York.
