89967-18-0 Usage
Uses
Used in Pharmaceutical Industry:
4-PROPYL-6-HYDROXY-2-METHYLPYRIMIDINE is used as a building block in the synthesis of pharmaceutical drugs. Its unique structure allows it to be a key component in the development of new medications, potentially contributing to the treatment of various diseases and conditions.
Used in Agrochemical Products:
4-PROPYL-6-HYDROXY-2-METHYLPYRIMIDINE is also used as a potential active ingredient in agrochemical products. Its incorporation into these products can help improve their effectiveness in agricultural applications, such as pest control and crop protection, thereby enhancing overall crop yield and quality.
Check Digit Verification of cas no
The CAS Registry Mumber 89967-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,6 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89967-18:
(7*8)+(6*9)+(5*9)+(4*6)+(3*7)+(2*1)+(1*8)=210
210 % 10 = 0
So 89967-18-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2O/c1-3-4-7-5-8(11)10-6(2)9-7/h5H,3-4H2,1-2H3,(H,9,10,11)
89967-18-0Relevant academic research and scientific papers
TRIAZOLOPYRIMIDINE DERIVATIVES WHICH ARE ANGIOTENSIN II RECEPTOR ANTAGONISTS
-
, (2008/06/13)
The present invention relates to the derivatives of formula: STR1 and to their tautomeric forms as well as to their addition salts and to their use in therapy, in particular for the treatment of cardiovascular diseases, especially for the treatment of hypertension, cardiac insufficiency and diseases of the arterial wall.
Studies on Pyrimidine Derivatives. XXXIII. Synthesis of Alkyl Pyrimidinyl Ketones by Means of Nitrosation of Alkylpyrimidines
Sakamoto, Takao,Sakasai, Takeji,Yoshizawa, Hiroshi,Tanji, Ken-Ichi,Nishimura, Sumiko,Yamanaka, Hiroshi
, p. 4554 - 4560 (2007/10/02)
The reaction of 4-alkylpyrimidines with propyl nitrite under acidic conditions followed by deoximation of the resulting ketoximes gave alkyl pyrimidinyl ketones in satisfactory yields.As compared with the direct oxidation of the alkylpyrimidines with sele
