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 academic research and scientific papers
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.
An efficient catalytic method for the Beckmann rearrangement of ketoximes to amides and aldoximes to nitriles mediated by propylphosphonic anhydride (T3P)
Augustine, John Kallikat,Kumar, Rajesha,Bombrun, Agnes,Mandal, Ashis Baran
experimental part, p. 1074 - 1077 (2011/03/22)
An efficient method for the Beckmann rearrangement of ketoximes to amides mediated by a catalytic amount (15 mol %) of propylphosphonic anhydride (T3P) is described. Aldoximes underwent second order Beckmann rearrangement to provide the corresponding nitriles in excellent yields on reacting with T3P (15 mol %) at room temperature. The main advantages of this environmentally friendly protocol include procedural simplicity, and particularly ease of isolation of the products.
