1677-49-2 Usage
General Description
2,4,7-trichloroquinoline is a chemical compound that contains three chlorine atoms attached to a quinoline ring structure. It is a halogenated aromatic compound and has a molecular formula of C9H4Cl3N. This chemical is commonly used in the synthesis of pharmaceuticals and agrochemicals due to its unique structural properties and reactivity. It has also been investigated for its potential use as a fluorescent dye in biological and environmental applications. Additionally, 2,4,7-trichloroquinoline is known to have moderate toxicity and should be handled and used with caution in laboratory and industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 1677-49-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,7 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1677-49:
(6*1)+(5*6)+(4*7)+(3*7)+(2*4)+(1*9)=102
102 % 10 = 2
So 1677-49-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H4Cl3N/c10-5-1-2-6-7(11)4-9(12)13-8(6)3-5/h1-4H
1677-49-2Relevant articles and documents
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Lutz et al.
, p. 1285,1288 (1946)
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Regioselective synthesis of novel 2-chloroquinoline derivatives of 1,4-dihydropyridines
Rajesh,Iniyavan,Sarveswari,Vijayakumar
, p. 1851 - 1866 (2014/05/06)
Highly regioselective reaction of some substituted 2,4-dichloroquinolines with symmetrical 1,4-dihydropyridines, leading to novel quinoline derivatives of DHPs, has been achieved in the presence of powdered K2CO 3, as a mild and efficient base, at moderate temperature. All the synthesized compounds were characterized by use of IR, NMR, and mass spectral data.
SUBSTITUTED QUINOLINE CCR5 RECEPTOR ANTAGONISTS
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Page 67-68, (2010/02/06)
The present invention relates to CCR5 receptor antagonists of formulae (1a) or (1b), enantiomers, diastereomers, salts and solvates thereof wherein R1, R2, R3, R4, R5, and R7 are as defined herein. The invention further includes a method of CCR5-mediated