26990-69-2 Usage
Uses
Used in Pharmaceutical Industry:
1,3-DIMETHYL-5-MORPHOLINO-1H-PYRAZOLE-4-CARBALDEHYDE is utilized as an intermediate in the synthesis of various drugs and organic compounds. Its versatile reactivity and structural properties make it a valuable component in the development of new pharmaceuticals.
Used in Organic Synthesis:
As a building block in organic synthesis, 1,3-DIMETHYL-5-MORPHOLINO-1H-PYRAZOLE-4-CARBALDEHYDE is employed for creating a wide range of organic compounds. Its unique structural features contribute to the formation of diverse chemical entities with potential applications in various fields.
Used in Material Development:
Due to its unique structural properties, 1,3-DIMETHYL-5-MORPHOLINO-1H-PYRAZOLE-4-CARBALDEHYDE may have potential applications in the development of new materials. Its incorporation into material formulations could lead to the creation of innovative products with enhanced properties.
Check Digit Verification of cas no
The CAS Registry Mumber 26990-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,9 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 26990-69:
(7*2)+(6*6)+(5*9)+(4*9)+(3*0)+(2*6)+(1*9)=152
152 % 10 = 2
So 26990-69-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H15N3O2/c1-8-9(7-14)10(12(2)11-8)13-3-5-15-6-4-13/h7H,3-6H2,1-2H3
26990-69-2Relevant academic research and scientific papers
Identification of antitumor activity of pyrazole oxime ethers
Park, Hyun-Ja,Lee, Kyung,Park, Su-Jin,Ahn, Bangle,Lee, Jong-Cheol,Cho, HeeYeong,Lee, Kee-In
, p. 3307 - 3312 (2007/10/03)
A series of pyrazole oxime ether derivatives were prepared and examined as cytotoxic agents. In particular, 5-phenoxypyrazole was comparable to doxorubicin, while exhibiting very potent cytotoxicity against XF 498 and HCT15.
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.
