884507-42-0 Usage
Uses
Used in Pharmaceutical Industry:
3-(PYRROLIDIN-1-YLMETHYL)BENZALDEHYDE 97 is used as a key intermediate in the synthesis of pharmaceuticals for its ability to be readily incorporated into complex molecular structures. Its unique chemical properties make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-(PYRROLIDIN-1-YLMETHYL)BENZALDEHYDE 97 is utilized as a starting material for the preparation of various agrochemicals. Its role in this industry is crucial for the creation of compounds that can be used in pest control and crop protection, contributing to enhanced agricultural productivity and sustainability.
It is important to handle 3-(PYRROLIDIN-1-YLMETHYL)BENZALDEHYDE 97 with care due to its potential harmful effects if ingested, inhaled, or comes into contact with the skin or eyes. Proper safety measures should be taken during its use to ensure the well-being of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 884507-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,4,5,0 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 884507-42:
(8*8)+(7*8)+(6*4)+(5*5)+(4*0)+(3*7)+(2*4)+(1*2)=200
200 % 10 = 0
So 884507-42-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO/c14-10-12-5-3-4-11(8-12)9-13-6-1-2-7-13/h3-5,8,10H,1-2,6-7,9H2
884507-42-0Relevant articles and documents
METHODS OF PREPARING TOLL-LIKE RECEPTOR MODULATORS
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, (2016/04/09)
The present invention provides methods of preparing 4-amino-2-biitoxy-8-(3- (pyrrolidin-1-ylmethyl)benzyl)-7,8-dihydropteridin-6(5H)-one and related compounds.
MODULATORS OF TOLL-LIKE RECEPTORS
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Page/Page column 44, (2010/06/19)
Provided are modulators of TLRs of Formula II: pharmaceutically acceptable salts thereof, compositions containing such compounds, and therapeutic methods that include the administration of such compounds.
Design, synthesis and AChE inhibitory activity of indanone and aurone derivatives
Sheng, Rong,Xu, Yu,Hu, Chunqi,Zhang, Jing,Lin, Xiao,Li, Jingya,Yang, Bo,He, Qiaojun,Hu, Yongzhou
experimental part, p. 7 - 17 (2009/04/06)
A new series of indanone and aurone derivatives have been synthesized and tested for in vitro AChE inhibitory activity by modified Ellman method. Most of them exhibit AChE inhibitory activities superior to rivastigmine. Further, the most potent compound 1g was selected to evaluate the effect on the acquisition and memory impairment by mice step-down passive avoidance test.
