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1H-Pyrrolizine, 2,3-dihydro-5-methyl-(7CI,8CI,9CI) is a chemical compound belonging to the pyrrolizine family. It is a naturally occurring alkaloid found in various plants, particularly in the genus Lobelia. 1H-Pyrrolizine,2,3-dihydro-5-methyl-(7CI,8CI,9CI) is characterized by its unique structure, which consists of a pyrrolizine ring fused to a dihydro-2,3-dihydro-5-methyl group. The compound is known for its potential biological activities, such as its use as a research tool in studying the effects of alkaloids on the central nervous system. It is also used in the synthesis of other related compounds with potential therapeutic applications. Due to its complex structure and potential applications, 1H-Pyrrolizine, 2,3-dihydro-5-methyl-(7CI,8CI,9CI) is an important compound in the field of organic chemistry and pharmacology.

7312-34-7

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7312-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7312-34-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,1 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7312-34:
(6*7)+(5*3)+(4*1)+(3*2)+(2*3)+(1*4)=77
77 % 10 = 7
So 7312-34-7 is a valid CAS Registry Number.

7312-34-7Downstream Products

7312-34-7Relevant academic research and scientific papers

Pyrrole synthesis catalyzed by AgOTf or cationic Au(I) complexes

Harrison, Tyler J.,Kozak, Jennifer A.,Corbella-Pane, Montserrat,Dake, Gregory R.

, p. 4525 - 4529 (2007/10/03)

Either silver trifluoromethanesulfonate or a mixture of gold(I) chloride, silver trifluoromethanesulfonate, and triphenylphosphine catalyze the formation of pyrroles from substituted β-alkynyl ketones and amines. The reactions proceed by using 5 mol % of catalyst with yields of isolated pyrroles ranging from 13% to 92%. Sixteen examples are used to compare the effectiveness of each catalyst.

Reaction of N-acylated isofebrifugine with acid

Takeuchi, Yasuo,Azuma, Kumiko,Abe, Hitoshi,Harayama, Takashi

, p. 2247 - 2252 (2007/10/03)

The reaction of N-acylated isofebrifugine with hydrochloric acid is discussed. Although the corresponding deprotected compound was not isolated, three new heterocyclic compounds were obtained. Based on these findings, new furan and pyrrole derivatives wer

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