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160233-76-1

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160233-76-1 Usage

General Description

6-Bromoquinoline-4-carboxylic acid is a chemical compound with the molecular formula C10H6BrNO2. It is a derivative of quinoline, a heterocyclic aromatic compound, and is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. 6-Bromoquinoline-4-carboxylic acid has a bromine atom and a carboxylic acid functional group attached to the quinoline ring. It is also known for its potential biological activities, such as antiviral, antibacterial, and anticancer properties. Additionally, it can be utilized in the development of fluorescent dyes and as a reagent in organic chemistry. Overall, 6-Bromoquinoline-4-carboxylic acid has various applications in both the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 160233-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,2,3 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 160233-76:
(8*1)+(7*6)+(6*0)+(5*2)+(4*3)+(3*3)+(2*7)+(1*6)=101
101 % 10 = 1
So 160233-76-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H6BrNO2/c11-6-1-2-9-8(5-6)7(10(13)14)3-4-12-9/h1-5H,(H,13,14)

160233-76-1Downstream Products

160233-76-1Relevant articles and documents

Synthesis and biological evaluation of novel 4-(6-substituted quinolin-4-yl)-N-aryl thiazol-2-amine derivatives as potential antimicrobial agents

Thakare, Prashant,Shinde, Abhijit,Dakhane, Sagar,Chavan, Abhijit,Bobade, Vivek D.,Mhaske, Pravin C.

, p. 1867 - 1877 (2021)

Cyclocondensation reaction of 4-(2-bromoacetyl)quinolin-1-ium bromide (4a–d) with substituted arylthiourea, (5a–g) afforded 4-(6-substituted quinolin-4-yl)-N-aryl/pyridyl thiazol-2-amine (6a-ab). These newly synthesized derivatives were evaluated for in vitro antibacterial activity against Escherichia coli (NCIM 2574), Proteus mirabilis (NCIM 2388) (Gram-negative strains), Bacillus subtilis (NCIM 2063), Staphylococcus albus (NCIM 2178) (Gram-positive strains) and in vitro antifungal activity against Aspergillus niger (ATCC 504) and Candida albicans (NCIM 3100). Compounds 6a, 6b, 6d, 6f, 6k, and 6l showed moderate to good antibacterial activity against S. albus. Ten derivatives 6c, 6q, 6r, 6s, 6t, 6v, 6w, 6x, 6y, and 6aa, showed moderate to good activity against A. niger. N-[4-(Quinolin-4-yl)-1,3-thiazol-2-yl]pyridin-2-amine presented comparable activity against A. niger with respect to standard drug Rouconazole.

Quinoline formamide compound as well as preparation method and application thereof

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Paragraph 0130-0132; 0136-0138, (2020/11/25)

The invention discloses quinoline formamide compounds as well as a preparation method and application thereof. Specifically, the invention relates to a compound represented by a formula (I) as shown in the specification or a tautomer, a meso-racemate, a r

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