37110-15-9 Usage
Explanation
The compound consists of 6 carbon atoms, 7 hydrogen atoms, 1 nitrogen atom, and 1 oxygen atom.
Explanation
1-Methyl-1H-pyrrole-2-carbaldehyde oxime is derived from pyrrole-2-carbaldehyde by attaching an oxime group.
Explanation
The compound is commonly referred to as "Pyrolin" in scientific literature.
Explanation
1-Methyl-1H-pyrrole-2-carbaldehyde oxime is used as a building block for various heterocyclic compounds in organic synthesis.
Explanation
The compound is used as a reagent in the synthesis of pyrrole-2-carboxylic acid derivatives, which have potential pharmaceutical applications.
Explanation
1-Methyl-1H-pyrrole-2-carbaldehyde oxime has been studied for its potential role in the treatment of various diseases, particularly as an anti-inflammatory and antioxidant agent.
Explanation
The compound is used in the synthesis of other important chemicals, such as vitamin B6 and some anti-tuberculosis (TB) drugs.
Oxime derivative
pyrrole-2-carbaldehyde
Use in organic synthesis
building block for heterocyclic compounds
Use in pharmaceutical research
synthesis of pyrrole-2-carboxylic acid derivatives
Potential therapeutic applications
anti-inflammatory and antioxidant agent
Synthesis of other important chemicals
vitamin B6 and anti-TB drugs
Check Digit Verification of cas no
The CAS Registry Mumber 37110-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,1 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 37110-15:
(7*3)+(6*7)+(5*1)+(4*1)+(3*0)+(2*1)+(1*5)=79
79 % 10 = 9
So 37110-15-9 is a valid CAS Registry Number.
37110-15-9Relevant articles and documents
Radical-anion coupling through reagent design: hydroxylation of aryl halides
Chechik, Victor,Greener, Andrew J.,James, Michael J.,Oca?a, Ivan,Owens-Ward, Will,Smith, George,Ubysz, Patrycja,Whitwood, Adrian C.
, p. 14641 - 14646 (2021/11/17)
The design and development of an oxime-based hydroxylation reagent, which can chemoselectively convert aryl halides (X = F, Cl, Br, I) into phenols under operationally simple, transition-metal-free conditions is described. Key to the success of this approach was the identification of a reducing oxime anion which can interact and couple with open-shell aryl radicals. Experimental and computational studies support the proposed radical-nucleophilic substitution chain mechanism.
Synthesis of platinum complexes of 2-aminomethylpyrrolidine derivatives for use as carrier ligands and their antitumor activities
Morikawa,Honda,Endoh,Matsumoto,Akamatsu,Mitsui,Koizumi
, p. 930 - 935 (2007/10/02)
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