90689-39-7 Usage
Description
(1-Oxo-1H-phthalazin-2-yl)-acetic acid, also known as phthalazinacetic acid, is a chemical compound with the molecular formula C10H9NO3. It is a derivative of phthalazin, a heterocyclic aromatic compound. (1-OXO-1 H-PHTHALAZIN-2-YL)-ACETIC ACID is an acetic acid derivative with a phthalazin-2-one core, and it is used in organic synthesis and pharmaceutical research.
Uses
Used in Pharmaceutical Research:
(1-Oxo-1H-phthalazin-2-yl)-acetic acid is used as a building block in the synthesis of various organic compounds for pharmaceutical research. Its unique structure and potential biological activities make it an interesting target for the development of new pharmaceutical drugs.
Used in Organic Synthesis:
In the field of organic synthesis, (1-Oxo-1H-phthalazin-2-yl)-acetic acid is used as a key intermediate for the synthesis of a wide range of organic compounds. Its versatile chemical properties allow it to be incorporated into various molecular structures, making it a valuable component in the creation of new chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 90689-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,8 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90689-39:
(7*9)+(6*0)+(5*6)+(4*8)+(3*9)+(2*3)+(1*9)=167
167 % 10 = 7
So 90689-39-7 is a valid CAS Registry Number.
90689-39-7Relevant articles and documents
Phthalazinone in heterocyclic synthesis: Synthesis of some s-triazole, s-triazolothiadiazine, s-triazolothiadiazine, and s-triazolothiadiazole derivatives as pharmaceutical interest
Hassanien, Abu Zeid Abd El-Baset
, p. 1987 - 1997 (2007/10/03)
1(2H)-Oxophthalazine-2-acetic acid ethyl ester was allowed to react with various reagents under different conditions to yield compounds 2-[(4-substituted-5-mercaptotriazol-3-yl) methyl]-1(2H)-oxophthalzines 5 and 7 which acted as starting materials for the preparation of some new s-triazolo[5,1-b][1,3]thiazine (8), s-triazolo[3,4-b][1,3,4]thiadiazine 9,12,14,20, and s-triazolo[3,4-b][1,3,4]thiadiazole 18,21 derivatives.