33317-03-2 Usage
Uses
Used in Pharmaceutical Synthesis:
Methyl 4,5-dimethyl-1H-pyrrole-2-carboxylate is utilized as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and medications.
Used in Agrochemical Production:
Methyl4,5-dimethyl-1H-pyrrole-2-carboxylate also serves as an intermediate in the production of agrochemicals, playing a role in the creation of substances that protect crops and enhance agricultural productivity.
Used in Organic Compounds Synthesis:
Methyl 4,5-dimethyl-1H-pyrrole-2-carboxylate is employed in the synthesis of various organic compounds, expanding the range of chemical products available for different applications.
Used in Fragrance and Flavor Industry:
As an intermediate, it is used in the production of fragrances and flavors, adding to the complexity and variety of scents and tastes in consumer products.
Used in Materials Science:
Methyl 4,5-dimethyl-1H-pyrrole-2-carboxylate has potential applications in materials science, particularly in the development of polymers and coatings, where its unique properties can enhance material performance.
Safety Note:
Due to its flammable nature and potential to cause skin and eye irritation, Methyl 4,5-dimethyl-1H-pyrrole-2-carboxylate should be handled with care to ensure safety during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 33317-03-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,3,1 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33317-03:
(7*3)+(6*3)+(5*3)+(4*1)+(3*7)+(2*0)+(1*3)=82
82 % 10 = 2
So 33317-03-2 is a valid CAS Registry Number.
33317-03-2Relevant academic research and scientific papers
Catalytic asymmetric hydrogenation of 2,3,5-trisubstituted pyrroles
Kuwano, Ryoichi,Kashiwabara, Manabu,Ohsumi, Masato,Kusano, Hiroki
, p. 808 - 809 (2008/09/20)
Catalytic asymmetric hydrogenation of N-Boc-protected pyrroles proceeded with high enantioselectivity by using a ruthenium catalyst modified with a trans-chelating chiral bisphosphine PhTRAP. The ruthenium catalyst prepared from Ru(η3-methallyl
Pyrrolopyridazine derivatives
-
, (2008/06/13)
Pyrrolopyridazine derivatives having the general formula. In the above formula, R1 represents a C2-C6alkenyl-group, a halogeno-C2-C6-alkenyl group, a C6-C10 aryl-C2-C6-alkenyl group, a C2-C6 alkynyl group, a C3-C7 cycloalkyl group, a C3-C7 cycloalkyl-C1-C6-alkyl group, a C5-C7 cycloalkenyl-C1-C6-alkyl group or a halogeno-C1-C6-alkyl group; R2 and R3 are the same or different and each represents a hydrogen atom, a C1-C6 alkyl group or a C6-C10 aryl group; R4 represents a hydrogen atom or a C1-C6 alkyl group; R5 represents a C6-C10 aryl group or a 5-10 membered heteroaryl group comtaining heteroatom(s) selected from nitrogen, oxygen and sulfur;
