38707-70-9 Usage
Description
8-Quinolinecarbaldehyde is an off-white solid that serves as a crucial intermediate in various chemical syntheses. It is widely recognized for its significance in the production of organic compounds, pharmaceuticals, agrochemicals, and dyes.
Uses
Used in Organic Synthesis:
8-Quinolinecarbaldehyde is used as a key intermediate for the synthesis of various organic compounds. Its unique chemical structure allows for the creation of a broad range of products, making it a valuable asset in this field.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 8-Quinolinecarbaldehyde is utilized as a vital building block for the development of new drugs. Its properties enable the design and synthesis of innovative pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemicals:
8-Quinolinecarbaldehyde is employed as a raw material in the agrochemical sector, where it is used to develop novel compounds for pest control and crop protection. Its role in this industry is essential for enhancing agricultural productivity and ensuring food security.
Used in Dyestuff Industry:
In the dyestuff industry, 8-Quinolinecarbaldehyde is used as a starting material for the production of various dyes. Its chemical properties make it suitable for creating a wide array of colorants used in different applications, such as textiles, plastics, and printing inks.
Check Digit Verification of cas no
The CAS Registry Mumber 38707-70-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,0 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38707-70:
(7*3)+(6*8)+(5*7)+(4*0)+(3*7)+(2*7)+(1*0)=139
139 % 10 = 9
So 38707-70-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H7NO/c12-7-9-4-1-3-8-5-2-6-11-10(8)9/h1-7H
38707-70-9Relevant articles and documents
Metal Ion-Driven Constitutional Adaptation in Dynamic Covalent C=C/C=N Organo-Metathesis
Gu, Ruirui,Lehn, Jean-Marie
, p. 44 - 48 (2020/12/09)
Knoevenagel barbiturate derivatives and imines are able to undergo efficient component recombination through dynamic covalent C=C/C=N organo-metathesis in absence of a catalyst. A [2×2] dynamic covalent library (DCL) containing two Knoevenagel derivatives Kn1 and Kn2 and two imines A1 and A2 has been established and its adaptive features in response to the addition of metal cations have been investigated. Addition of Cu(I) triflate as an effector, induces fast and remarkable constitutional selection of the DCL towards amplification of the Cu(I)-A2 complex and its agonist Kn1. This adaptation process could be reversed by addition of neocuproine as a competitive Cu(I) ligand. Furthermore, separate addition of five other metal cations as input agents, i. e. Ag(I), Fe(II), Zn(II), Cu(II) and Li(I), led to the generation of cation-specific distribution patterns as outputs, showing the ability of the present DCL to recognize different effectors.
