34660-61-2 Usage
Chemical Class
Pyrrole derivatives
Explanation
1H-Pyrrole, 2-(2-furanylmethyl)is a compound that belongs to the class of pyrrole derivatives, which are heterocyclic organic compounds containing a pyrrole ring.
2. Heterocyclic Compound
Explanation
It contains a pyrrole ring and a furan group, making it a heterocyclic compound with atoms other than carbon, such as nitrogen and oxygen, in its ring structure.
Explanation
1H-Pyrrole, 2-(2-furanylmethyl)has potential applications in the pharmaceutical industry due to its various biological activities, including antimicrobial, antifungal, and anticancer properties.
4. Applications in Agriculture
Explanation
The compound has potential applications in the agricultural industry, possibly due to its antimicrobial and antifungal properties, which could be useful in controlling pests and diseases in crops.
5. Synthesis of Bioactive Compounds
Explanation
1H-Pyrrole, 2-(2-furanylmethyl)is used in the synthesis of various bioactive compounds, making it a valuable building block in organic chemistry.
6. Building Block in Organic Chemistry
Explanation
The compound serves as a building block in organic chemistry, allowing for the creation of more complex molecules and compounds with potential applications in various industries.
Biological Activities
Antimicrobial, antifungal, and anticancer properties
Check Digit Verification of cas no
The CAS Registry Mumber 34660-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,6 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34660-61:
(7*3)+(6*4)+(5*6)+(4*6)+(3*0)+(2*6)+(1*1)=112
112 % 10 = 2
So 34660-61-2 is a valid CAS Registry Number.
34660-61-2Relevant academic research and scientific papers
ALKYLATION OF FURAN, THIOPHENE, AND PYRROLE WITH FURFURYL ALCOHOL IN THE PRESENCE OF THE STRONGLY ACIDIC AMBERLYST 15 SULFO CATION-EXCHANGE RESIN
Iovel', I. G.,Gol'dberg, Yu. Sh.,Shimanskaya, M. V.
, p. 613 - 616 (2007/10/02)
The corresponding 2-furylhetarylmethanes were obtained by the reaction of furan, thiophene, or pyrrole with furfuryl alcohol in the presence of the strongly acidic Amberlyst 15 cation-exchange resin in the H+ form.The alkylation of furan and thiophene takes place regiospecifically in the 2 position, whereas 2-furyl-2-pyrrolyl- and 2-furyl-3-pyrrolylmethane in a ratio of 6.2:1 are formed in the case of pyrrole.
