161282-57-1 Usage
Description
Tert-butyl 2-formyl-1H-pyrrole-1-carboxylate is a chemical compound that belongs to the pyrrole carboxylate family. It is a derivative of pyrrole and is known for its unique chemical properties. tert-Butyl 2-formyl-1H-pyrrole-1-carboxylate is commonly used in organic synthesis and pharmaceutical research, serving as a building block in the synthesis of bioactive molecules. Its versatile nature and reactivity make it a valuable tool in the development of new and innovative compounds for various research and industrial purposes.
Uses
Used in Pharmaceutical Research:
Tert-butyl 2-formyl-1H-pyrrole-1-carboxylate is used as a key intermediate in the synthesis of pharmaceutical compounds for various therapeutic applications. Its unique chemical structure allows for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, tert-butyl 2-formyl-1H-pyrrole-1-carboxylate is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity and chemical properties enable the creation of effective and targeted agrochemicals for crop protection and management.
Used in Organic Synthesis:
Tert-butyl 2-formyl-1H-pyrrole-1-carboxylate is utilized as a versatile building block in organic synthesis, allowing for the creation of a wide range of organic compounds with diverse applications. Its unique structure and reactivity contribute to the development of novel organic compounds for various industries, including materials science, chemical engineering, and specialty chemicals.
Used in Research and Development:
Due to its unique chemical properties and reactivity, tert-butyl 2-formyl-1H-pyrrole-1-carboxylate is a sought-after compound in research and development. It is used to explore new chemical reactions, investigate novel synthetic pathways, and develop innovative compounds with potential applications in various fields, such as medicine, agriculture, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 161282-57-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,2,8 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 161282-57:
(8*1)+(7*6)+(6*1)+(5*2)+(4*8)+(3*2)+(2*5)+(1*7)=121
121 % 10 = 1
So 161282-57-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO3/c1-10(2,3)14-9(13)11-6-4-5-8(11)7-12/h4-7H,1-3H3
161282-57-1Relevant articles and documents
Concise synthesis of multisubstituted isoquinolines from pyridines by regioselective diels-alder reactions of 2-silyl-3,4-pyridynes
Ikawa, Takashi,Urata, Hirohito,Fukumoto, Yutaka,Sumii, Yuta,Nishiyama, Tsuyoshi,Akai, Shuji
, p. 16228 - 16232 (2014)
A four-step regioselective synthesis of multisubsti-tuted isoquinoline derivatives from 3-bromopyridines was developed by the Diels-Alder (DA) reactions of 2-silyl-3,4-pyridynes with furans, followed by functional-group transformations. In particular, the silyl group at the C2-position of the 3,4-pyridynes played two important roles: firstly, it functioned as the directing group for the DA reaction, and secondly, it served to introduce diverse substituents at the C1-position of the isoquinolines by electrophilic ipso-substitution.
Addition of Chloroprene Grignards to Aromatic Aldehydes: Synthesis of Homoallenyl Alcohols
Geissler, Arne G. A.,Breit, Bernhard
supporting information, p. 2621 - 2625 (2021/04/12)
A general procedure for the one-pot synthesis of racemic homoallenyl alcohols from the corresponding aldehyde and chloroprene-derived Grignards is described. Employing bis[2-dimethylaminoethyl]ether (BDMAEE) as an additive at low temperatures shifts the selectivity of the chloroprene Grignard addition to aldehydes such that it is almost exclusive toward allene formation. In a set of follow-up experiments, simple and more elaborate methods for further derivatization have been demonstrated, allowing quick access to more complex structures.
Serendipitous base catalysed condensation-heteroannulation of iminoesters: a regioselective route to the synthesis of 4,6-disubstituted 5-azaindoles
Chelvam, Venkatesh,Dudhe, Premansh,Pathak, Biswarup,Venkatasubbaiah, Krishnan
supporting information, p. 1582 - 1587 (2020/03/06)
A serendipitous discovery of a novel one-pot synthesis of 4,6-disubstituted 5-azaindoles is reported herein. In the presence of Hunig's base, various N-substituted pyrrole-2-carboxaldehydes have been efficiently transformed into their corresponding 4,6-disubstituted 5-azaindoles through an imine mediated cascade condensation-heteroannulation. The synthetic value of the methodology is established by preparing a novel chemical analogue of a cannabinoid receptor type 2 (CB2) agonist.
