114374-36-6 Usage
General Description
1H-Pyrrole, 1-(1-oxo-2-propenyl)-(9CI) is a chemical compound with the molecular formula C7H7NO. It is a member of the pyrrole family, a five-membered aromatic heterocycle that contains a nitrogen atom in the ring. The compound is also known as 1-acetyl-1H-pyrrole and is commonly used in organic synthesis as a starting material for the preparation of various other compounds. It is a colorless to pale yellow liquid with a pungent odor and is soluble in organic solvents such as ethanol and ether. 1H-Pyrrole,1-(1-oxo-2-propenyl)-(9CI) has potential applications in the pharmaceutical and agrochemical industries, serving as a building block for the synthesis of biologically active molecules and as a precursor for the development of new pesticide and fungicide products.
Check Digit Verification of cas no
The CAS Registry Mumber 114374-36-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,7 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 114374-36:
(8*1)+(7*1)+(6*4)+(5*3)+(4*7)+(3*4)+(2*3)+(1*6)=106
106 % 10 = 6
So 114374-36-6 is a valid CAS Registry Number.
114374-36-6Relevant articles and documents
Alternate syntheses of prodan and acrylodan
Silvonek, Steven S.,Giller, Carl B.,Abelt, Christopher J.
, p. 589 - 594 (2005)
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Enantioselective organocatalytic Michael additions to acrylic acid derivatives: Generation of all-carbon quaternary stereocentres
Rigby, Caroline L.,Dixon, Darren J.
supporting information; experimental part, p. 3798 - 3800 (2009/02/07)
Acrylic esters, thioesters and N-acryloyl pyrrole have been identified as effective electrophiles in the enantioselective Michael addition reaction with β-keto ester pro-nucleophiles catalysed by a cinchona alkaloid derived bifunctional organocatalyst; enantiomeric excesses of up to 98% and yields of up to 96% can be obtained for a range of Michael acceptors and pro-nucleophiles. The Royal Society of Chemistry.
