33369-47-0 Usage
Uses
Used in Pharmaceutical Synthesis:
Ethyl 1,4-dimethyl-1H-pyrrole-2-acetate is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a valuable building block for the development of new drugs with potential therapeutic applications.
Used in Fine Chemicals Production:
This chemical compound is also utilized in the production of fine chemicals, which are high-purity chemicals used in various industries such as fragrances, flavors, and agrochemicals.
Used in Organic Electronics:
Ethyl 1,4-dimethyl-1H-pyrrole-2-acetate may have potential applications in the field of organic electronics, where its unique properties could contribute to the development of new electronic materials and devices.
Safety Precautions:
It is crucial to handle ethyl 1,4-dimethyl-1H-pyrrole-2-acetate with care and follow proper safety precautions when working with this chemical to ensure the safety of both individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 33369-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,3,6 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33369-47:
(7*3)+(6*3)+(5*3)+(4*6)+(3*9)+(2*4)+(1*7)=120
120 % 10 = 0
So 33369-47-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO2/c1-4-13-10(12)6-9-5-8(2)7-11(9)3/h5,7H,4,6H2,1-3H3
33369-47-0Relevant articles and documents
Synthesis of Pyrroles through Rhodium(III)-Catalyzed Reactions of Allylamines and Alkenes
Kim, Dong-Su,Seo, Yong-Sik,Jun, Chul-Ho
supporting information, p. 3842 - 3845 (2015/08/18)
Pyrrole derivatives are generated in reactions of allylamines with alkenes that are promoted by a Rh(III) catalyst in the presence of AgOAc. This process, which involves chelation assisted C-H bond activation and N-annulation, is applied to a three step synthesis of Zomepirac.
1,3,6-trihydro-6-aza-3-oxapentalen-2-one derivatives for the treatment of neoplasia
-
, (2008/06/13)
1,3,6-Trihydro-6-Aza-3-Oxapentalen-2-One Derivatives for inhibiting neoplastic conditions.
Process for producing substituted pyrroles
-
, (2008/06/13)
Alkyl 1,4-dialkylpyrrole-2-alkanoates are prepared by the selective decarboxylation of a 1,4-dialkyl-3-carboxypyrrole-2-alkanoic acid or an alkyl ester or alkali metal salt thereof under moderate conditions with a mixture of a strong mineral acid, an alkanol, and water. The products are useful for the preparation of anti-inflammatory agents.
Process for preparing pyrrole-2-acetic acids
-
, (2008/06/13)
N-H and N-loweralkyl pyrrole-2-acetic acids are prepared by the reduction of 1-H and 1-loweralkyl-α-trichloromethylpyrrole-2-methanol with sodium dithionite (sodium hydrosulfite) in the presence of a base, MOH, wherein M is an alkali metal, an alkaline earth metal or tetraalkyl ammonium.
