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(6Z)-6-[4-(4-bromophenyl)-5-prop-2-enylsulfanyl-2H-1,2,4-triazol-3-yli dene]cyclohexa-2,4-dien-1-one is an organic compound characterized by its complex structure, featuring a cyclohexane ring with a substituted triazolylidene group and additional bromophenyl and prop-2-enylsulfanyl substituents. This yellow crystalline solid is of interest in medicinal chemistry research due to its potential as an anti-cancer or anti-inflammatory agent.

81518-40-3

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81518-40-3 Usage

Uses

Used in Pharmaceutical Research:
(6Z)-6-[4-(4-bromophenyl)-5-prop-2-enylsulfanyl-2H-1,2,4-triazol-3-yli dene]cyclohexa-2,4-dien-1-one is used as a research compound for its potential anti-cancer properties, given its unique structure and possible biological activity.
Used in Agrochemical Development:
(6Z)-6-[4-(4-bromophenyl)-5-prop-2-enylsulfanyl-2H-1,2,4-triazol-3-yli dene]cyclohexa-2,4-dien-1-one is also used as a starting material or intermediate in the development of new agrochemicals, where its specific structural features may contribute to novel pesticidal or herbicidal agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6Z)-6-[4-(4-bromophenyl)-5-prop-2-enylsulfanyl-2H-1,2,4-triazol-3-yli dene]cyclohexa-2,4-dien-1-one serves as a potential anti-inflammatory agent, which could be further optimized for therapeutic use in treating various inflammatory conditions.
Used in Drug Design and Synthesis:
(6Z)-6-[4-(4-bromophenyl)-5-prop-2-enylsulfanyl-2H-1,2,4-triazol-3-yli dene]cyclohexa-2,4-dien-1-one is utilized in drug design and synthesis processes, where its structural elements can be manipulated to create new pharmaceuticals with improved efficacy and reduced side effects.
Used in Chemical Synthesis:
(6Z)-6-[4-(4-bromophenyl)-5-prop-2-enylsulfanyl-2H-1,2,4-triazol-3-yli dene]cyclohexa-2,4-dien-1-one is used as a synthetic building block in the creation of more complex organic molecules, potentially leading to new classes of bioactive compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 81518-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,1 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81518-40:
(7*8)+(6*1)+(5*5)+(4*1)+(3*8)+(2*4)+(1*0)=123
123 % 10 = 3
So 81518-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H14BrN3OS/c1-2-11-23-17-20-19-16(14-5-3-4-6-15(14)22)21(17)13-9-7-12(18)8-10-13/h2-10,19H,1,11H2/b16-14+

81518-40-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-[4-(4-bromophenyl)-3-prop-2-enylsulfanyl-1H-1,2,4-triazol-5-ylidene]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:81518-40-3 SDS

81518-40-3Downstream Products

81518-40-3Relevant academic research and scientific papers

Synthesis and Antiinflammatory Activity of Some New 3-(o-Substituted phenyl)-4-substituted-phenyl-5-alkyl/alkenyl-mercapto-1H-1,2,4-triazoles

Tandon, M.,Barthwal, J. P.,Bhalla, T. N.,Bhargava, K. P.

, p. 1017 - 1018 (2007/10/02)

Eighteen 3-(o-substituted phenyl)-4-substituted-phenyl-5-alkyl/alkenyl-mercapto-1H-1,2,4-triazoles (IVa-r) have been synthesized by the reaction of 3-(o-substituted phenyl)-4-substituted-phenyl-5-mercapto-1H-1,2,4-triazoles (IIIa-d) with alkyl/alkenyl hal

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