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2H-Pyrrol-2-ol, 3,4-dihydro-3,3-dimethyl-5-(1-methylethyl)-(9CI) is a complex organic compound belonging to the pyrrole family. It is characterized by a five-membered heterocyclic ring with two hydrogen atoms attached to the nitrogen atom, making it a 2H-pyrrole derivative. The compound features a 3,4-dihydro structure, which means that there are two hydrogen atoms added to the carbon atoms at positions 3 and 4, resulting in a saturated ring. Additionally, it has two methyl groups (-CH3) attached to the carbon atom at position 3, and a 1-methylethyl (isopropyl) group (-CH(CH3)2) at position 5. This unique structure gives the compound specific chemical properties and potential applications in various fields, such as pharmaceuticals and agrochemicals.

338465-95-5

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338465-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 338465-95-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,8,4,6 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 338465-95:
(8*3)+(7*3)+(6*8)+(5*4)+(4*6)+(3*5)+(2*9)+(1*5)=175
175 % 10 = 5
So 338465-95-5 is a valid CAS Registry Number.

338465-95-5Downstream Products

338465-95-5Relevant academic research and scientific papers

3H-pyrroles, alkylidene-pyrrolines and functionalized pyrrolidines by radical cyclization of β-allenyliminyl radicals

Depature, Michael,Grimaldi, Jacques,Hatem, Jacques

, p. 941 - 946 (2007/10/03)

In this work, we show that the tin hydride-mediated reaction of allene-tethered dithiosemicarbazides 4 is a convenient method for the preparation of five-membered unsaturated nitrogen heterocycles. The sulfur-directed intermolecular attack of the tin radical at the semicarbazide moiety leads to an allene-tethered iminyl radical, which then undergoes a 5-exo-dig cyclization leading to both the 3H-pyrroles 5 and the alkylidene pyrrolines 6; thermal isomerization of 5 to 6 occurs in some cases.

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