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1H-Pyrazole-3-carboxylic acid, 5-benzoyl-1-(3-chlorophenyl)-4-(4-chlorophenyl)-4,5-dihydro-, ethyl ester, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144309-77-3

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144309-77-3 Usage

Molecular weight

421.25 g/mol

Structure

The compound contains a pyrazole ring, two benzene rings, a carboxylic acid group, a benzoyl group, and an ethyl ester functional group.

Configuration

The compound is in the transconfiguration, indicating the arrangement of the substituents on the double bond.

Properties

The specific properties of 1H-Pyrazole-3-carboxylic acid, 5-benzoyl-1-(3-chlorophenyl)-4-(4-chlorophenyl)-4,5-dihydro-, ethyl ester, trans- are not provided in the material. However, due to its complex structure and multiple functional groups, it may have a range of physical and chemical properties.

Applications

The specific applications of 1H-Pyrazole-3-carboxylic acid, 5-benzoyl-1-(3-chlorophenyl)-4-(4-chlorophenyl)-4,5-dihydro-, ethyl ester, trans- are not provided in the material. However, given its complex structure and multiple functional groups, it may have potential uses in fields such as pharmaceuticals, agrochemicals, or materials science. Further research and testing would be needed to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 144309-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,3,0 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 144309-77:
(8*1)+(7*4)+(6*4)+(5*3)+(4*0)+(3*9)+(2*7)+(1*7)=123
123 % 10 = 3
So 144309-77-3 is a valid CAS Registry Number.

144309-77-3Downstream Products

144309-77-3Relevant academic research and scientific papers

Nuclear megnetic resonance spectroscopy and the structures of the regioisomeric products of the cycloaddition of C-ethoxycarbonyl-N-arylnitrilimines to α,β-unsaturated ketones

Shawali, Ahmad S.,Ezmirly, Saleh T.,Bukhari, Ahmad M.

, p. 1165 - 1172 (2007/10/02)

(1)H NMR chemical shifts were used to assign the structures of the regioisomeric products obtained from the reactions of C-ethoxycarbonyl-N-arylnitrilimines 2A-E to α,β-unsaturated ketones 3a-j.The assignments were based on the large observed difference b

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