112565-44-3 Usage
Chemical structure
1H-Indole, 1-(phenylmethyl)-2-(2-pyrrolidinyl)is a chemical compound with an indole ring fused with a phenylmethyl group and a pyrrolidinyl group.
Usage
It is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and functional materials.
Biological activities
The presence of both the indole and pyrrolidinyl moieties in the molecule imparts it with unique biological activities and pharmacological properties.
Value in drug discovery
It is a valuable intermediate for drug discovery and development due to its unique biological activities and pharmacological properties.
Structural features
Its structural features, including the indole ring and the phenylmethyl and pyrrolidinyl groups, make it useful for the preparation of diverse heterocyclic compounds and functionalized indole derivatives.
Importance in organic synthesis
It is a versatile and important chemical in organic synthesis due to its ability to be used in the preparation of diverse heterocyclic compounds and functionalized indole derivatives.
Check Digit Verification of cas no
The CAS Registry Mumber 112565-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,5,6 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 112565-44:
(8*1)+(7*1)+(6*2)+(5*5)+(4*6)+(3*5)+(2*4)+(1*4)=103
103 % 10 = 3
So 112565-44-3 is a valid CAS Registry Number.
112565-44-3Relevant academic research and scientific papers
Synthesis of Some Hexahydroazocino indoles, a Tetra-and Two Hexahydropyrrolopyrroloindoles, and a Tetrahydropyrroloimidazoindole. Crystal Structure Determination of 1,2,3,4-Tetrahydro-2-Phenoxycarbonyl-7-phenylsu
Street, Jonathan D.,Harris, Martin,Bishop, David I.,Heatley, Frank,Beddoes, Roy L.,et al.
, p. 1599 - 1606 (2007/10/02)
Hexahydroazocinoindoles (2a-c) have been synthesised from 1-phenylsulphonylindole by introducing the appropriate side chain at C-2, via lithiation, and then intramolecular Mannich cyclisation.From (2c), 1,2,3,4-tetrahydro-2-phenoxycarbonyl-7-phenyl
