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methyl 3-methyl-1-phenyl-1H-thieno[2,3-c]pyrazole-5-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24086-28-0

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24086-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24086-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,8 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24086-28:
(7*2)+(6*4)+(5*0)+(4*8)+(3*6)+(2*2)+(1*8)=100
100 % 10 = 0
So 24086-28-0 is a valid CAS Registry Number.

24086-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-methyl-1-phenyl-1H-thieno[2,3-c]pyrazole-5-carboxylate

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:24086-28-0 SDS

24086-28-0Relevant academic research and scientific papers

Synthesis, biological evaluation and molecular docking studies of N-acylheteroaryl hydrazone derivatives as antioxidant and anti-inflammatory agents

Mahajan, Pravin S.,Nikam, Mukesh D.,Khedkar, Vijay M.,Jha, Prakash C.,Sarkar, Dhiman,Gill, Charansingh H.

, p. 2707 - 2729 (2016/03/19)

In search of new therapeutics with greater potency, three new series of 3-methyl-1-phenyl-1H-thieno[2,3-c]pyrazole-5-carbohydrazide derivatives have been synthesized and evaluated for their in vitro antioxidant and anti-inflammatory activities. The hydrazones bearing a core pyrazole, chromone and tetrazolo[1,5-a]quinoline scaffold showed promising activities. Interestingly, compounds 3a (EC50 = 06.00 ± 2.36) and 5c (EC50 = 07.21 ± 0.67) showed the most potent antioxidant activity, while compounds 3a (EC50 = 10.25 ± 1.08), 7b (EC50 = 10.50 ± 0.99) and 7c (EC50 = 11.18 ± 0.15) showed significant anti-inflammatory activity. Furthermore, molecular docking studies also revealed a significant correlation between the binding score and biological activity for these compounds to describe the molecular basis for the structure activity relationship (SAR) results. As these compounds are good cyclooxygenase inhibitors, isoenzyme inhibitory potency studies are warranted.

Novel synthesis of thieno[2, 3-c]pyrazoles and thieno[2, 3-d]pyrimidines

Ahluwalia, Vinod K.,Dahiya, Aruna,Bala, Madhu

, p. 715 - 717 (2007/10/03)

5 - Chloro - 4 - formyl - 3 - substitued -1 - phenyl - 1H-pyrazoles (1a-c) and 1, 3-diaryl-6-chloro-5-formyl-1, 3-dihydro-4-oxo-2-thioxopyrimidines (2a-f) on condensation with methyl thioglycolate furnish the corresponding methyl 3-aryl/alkyl-1-phenyl-1H-

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