137279-29-9 Usage
Uses
Used in Pharmaceutical Industry:
5-Pyrimidinecarboxaldehyde, 2-(ethylamino)(9CI) is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 5-Pyrimidinecarboxaldehyde, 2-(ethylamino)(9CI) serves as a crucial building block in the production of agrochemicals. Its reactivity and ethylamino group contribute to the creation of effective compounds for agricultural use.
Used in Organic Synthesis:
5-Pyrimidinecarboxaldehyde, 2-(ethylamino)(9CI) is utilized as a versatile building block in organic synthesis. Its unique structure and reactivity enable the formation of various heterocyclic compounds, which have a wide range of applications in different industries.
Used in Drug Development:
Due to its potential biological activity and pharmacological properties, 5-Pyrimidinecarboxaldehyde, 2-(ethylamino)(9CI) is employed in the development of new drugs. Its unique chemical structure allows for the exploration of novel therapeutic agents with improved efficacy and selectivity.
Used in Material Science:
5-Pyrimidinecarboxaldehyde, 2-(ethylamino)(9CI) also has potential applications in material science. Its unique chemical structure and reactivity can be harnessed to develop new materials with specific properties for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 137279-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,2,7 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 137279-29:
(8*1)+(7*3)+(6*7)+(5*2)+(4*7)+(3*9)+(2*2)+(1*9)=149
149 % 10 = 9
So 137279-29-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H9N3O/c1-2-8-7-9-3-6(5-11)4-10-7/h3-5H,2H2,1H3,(H,8,9,10)
137279-29-9Relevant academic research and scientific papers
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.
An Alternative Preparation of the 2-Dimethylaminomethylene-1,3-bis(dimethylimminio)propane Salt from Phosphonoacetic Acids and Some Applications in Heterocyclic Synthesis
Gupton, John T.,Gall, John E.,Riesinger, Steve W.,Smith, Stanton Q.,Bevirt, Kathy M.,et al.
, p. 1281 - 1285 (2007/10/02)
An alternative preparation of a 2-iminovinamidinium salt from phosphonoacetic acids is described along with its application to the synthesis of 5-formylpyrimidines and masked 4-formylpyrazoles.
