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5-dimethylamino-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde is a complex organic compound with the molecular formula C14H14N2O. It is a derivative of pyrazole, a five-membered heterocyclic ring containing nitrogen atoms, and features a phenyl group attached to the pyrazole ring. The molecule also has a dimethylamino group and a methyl group, which contribute to its unique chemical properties. 5-dimethylamino-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the creation of new molecules with specific biological activities. Its aldehyde functional group makes it a versatile intermediate in organic synthesis, allowing for further reactions to form a wide range of compounds.

5499-69-4

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5499-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5499-69-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,9 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5499-69:
(6*5)+(5*4)+(4*9)+(3*9)+(2*6)+(1*9)=134
134 % 10 = 4
So 5499-69-4 is a valid CAS Registry Number.

5499-69-4Relevant academic research and scientific papers

Facile microwave assisted decarbonylation of 4-formyl group in 5-alkyl amino substituted pyrazoles

Sakya, Subas M.,Abrams, Barbara,Snow, Sheri L.,Rast, Bryson

, p. 2280 - 2282 (2008/09/18)

Facile decarbonylation of the 4-formyl group in 5-alkyl amino pyrazoles was seen when reacted with catalytic p-toluene sulfonic acid in methanol under microwave irradiation to provide parent 4-H pyrazoles in good yields.

Introduction of N-containing heterocycles into pyrazole by nucleophilic aromatic substitution

Park, Min-Sup,Park, Hyun-Ja,Park, Koon Ha,Lee, Kee-In

, p. 1541 - 1550 (2007/10/03)

The nucleophilic aromatic substitution on 5-chloropyrazoles activated by the electron-withdrawing formyl group offers a useful method to introduce a wide range of N-containing heterocycles into them. The rate of reaction was greatly affected by the electronic nature of the N-1 substitution.

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