104461-06-5 Usage
Uses
Used in Pharmaceutical Industry:
5-Pyrimidinecarboxaldehyde, 2-(1,1-dimethylethyl)(9CI) is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and potential reactivity make it a valuable building block in the development of new drugs with specific therapeutic properties.
Used in Chemical Research:
In the field of chemical research, 5-Pyrimidinecarboxaldehyde, 2-(1,1-dimethylethyl)(9CI) serves as a subject of study to understand its properties, reactivity, and potential applications in various chemical reactions. Researchers can use 5-Pyrimidinecarboxaldehyde, 2-(1,1-dimethylethyl)- (9CI) to explore new reaction pathways and develop innovative synthetic methods.
Used in Material Science:
5-Pyrimidinecarboxaldehyde, 2-(1,1-dimethylethyl)(9CI) may find applications in material science, particularly in the development of novel materials with specific properties. Its unique structure and potential reactivity could contribute to the creation of advanced materials with applications in various industries, such as electronics, coatings, and adhesives.
Used in Agrochemical Industry:
In the agrochemical industry, 5-Pyrimidinecarboxaldehyde, 2-(1,1-dimethylethyl)(9CI) could be utilized as a starting material or intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its unique structure may offer new opportunities for the development of more effective and environmentally friendly agrochemical products.
Used in Dye and Pigment Industry:
5-Pyrimidinecarboxaldehyde, 2-(1,1-dimethylethyl)(9CI) may also find applications in the dye and pigment industry, where its unique structure and potential reactivity could be harnessed to develop new dyes and pigments with improved properties, such as colorfastness, stability, and solubility.
Check Digit Verification of cas no
The CAS Registry Mumber 104461-06-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,6 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104461-06:
(8*1)+(7*0)+(6*4)+(5*4)+(4*6)+(3*1)+(2*0)+(1*6)=85
85 % 10 = 5
So 104461-06-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O/c1-9(2,3)8-10-4-7(6-12)5-11-8/h4-6H,1-3H3
104461-06-5Relevant academic research and scientific papers
NMDA RECEPTOR MODULATORS AND USES THEREOF
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Paragraph 00166, (2018/07/29)
Disclosed herein, in part, are heteroaromatic compounds and methods of use in treating neuropsychiatric disorders, e.g., schizophrenia and major depressive disorder. Pharmaceutical compositions and methods of making heteroaromatic compounds are provided. The compounds are contemplated to modulate the NMDA receptor.
Shock sensitivity of a vinamidinium bis-perchlorate reagent and demonstration of a lower energy alternative
Ragan,McDermott,Jones,Am Ende,Clifford,McHardy,Heck,Liras,Segelstein
, p. 1172 - 1174 (2007/10/03)
'Vinamidinium' bis-perchlorate salt 1 (2-dimethylaminomethylene-1,3-bis(dimethylimmonio)-propane bis-perchlorate) was found to possess remarkably high thermal energy as well as significant shock sensitivity. A reported method for preparation of 2,5-disubstituted pyrimidines with 1 was of interest, and we found that the corresponding bis-tetrafluoroborate salt 2 was equally effective in this transformation, while possessing significantly lower thermal energy.
SYNTHESIS OF 1,3-DIHYDROFUROPYRIDINES AND 5,7-DIHYDROFUROPYRIDINES BY INTRAMOLECULAR DIELS-ALDER REACTIONS OF PYRIMIDINES. INVESTIGATION OF THE EFFECT OF STERIC INTERACTIONS ON THE REACTION RATE
Frissen, A. E.,Marcelis, A. T. M.,Buurman, D. G,Pollmann, C. A. M.,Plas, H. C. van der
, p. 5611 - 5620 (2007/10/02)
Several 2- and 5-propynyloxymethylpyrimidines were synthesized and their intramolecular Diels-Alder reaction was studied.The products of the reaction were 5,7-dihydrofuropyridines and 1,3-dihydrofuropyridines, respectively.Introduction of on
Pyrimidine substituted-2,2-dimethylcyclopropane carboxylates useful for combating insect and acarine pests at a locus
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, (2008/06/13)
A compound of formula: STR1 wherein R2 represents an α-branched alkyl group containing from 3 to 6 carbon atoms, and R represents either (a) hydroxy, halo or alkoxy of up to six carbon atoms, or (b) the group --OR1 where R1 is the residue of an alcohol of formula R1 OH which forms an insecticidal ester with chrysanthemic acid, permethrin acid or cyhalothrin acid. The compounds have insecticidal and acaricidal properties.
