13508-96-8 Usage
Description
2-Methyl-4-nitropyridine, with the CAS number 13508-96-8, is an organic compound characterized by its yellow solid appearance. It is known for its significance in the field of organic synthesis, where it serves as a key intermediate or building block for the creation of more complex molecules.
Uses
Used in Organic Synthesis:
2-Methyl-4-nitropyridine is used as a synthetic building block for the development of various organic compounds. Its unique structure and functional groups make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Methyl-4-nitropyridine is utilized as a key intermediate in the synthesis of drugs with potential therapeutic applications. Its presence in the molecular structure can contribute to the desired pharmacological properties of the final product.
Used in Agrochemical Industry:
2-Methyl-4-nitropyridine also finds application in the agrochemical industry, where it is employed in the synthesis of pesticides and other crop protection agents. Its incorporation into these compounds can enhance their effectiveness in protecting crops from pests and diseases.
Used in Dye and Pigment Industry:
The compound is also used as an intermediate in the production of dyes and pigments, where its chemical properties contribute to the color and stability of the final products.
Used in Research and Development:
2-Methyl-4-nitropyridine serves as a valuable research tool in academic and industrial laboratories, where it is used to study various chemical reactions and explore new synthetic pathways. Its versatility and reactivity make it an essential component in the development of novel chemical processes and products.
Check Digit Verification of cas no
The CAS Registry Mumber 13508-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,0 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13508-96:
(7*1)+(6*3)+(5*5)+(4*0)+(3*8)+(2*9)+(1*6)=98
98 % 10 = 8
So 13508-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O2/c1-5-4-6(8(9)10)2-3-7-5/h2-4H,1H3
13508-96-8Relevant articles and documents
The synthesis of 6-deazaformycin A
Tite, Tony,Lougiakis, Nikolaos,Marakos, Panagiotis,Pouli, Nicole
scheme or table, p. 2927 - 2930 (2010/02/28)
The synthesis of the new C-nucleoside 6-deazaformycin A was achieved through the condensation of a suitably substituted lithiated 2-picoline with 2,3,5-tri-O-benzyl-d-ribonolactone, borohydride reduction of the resulting hemiacetals, followed by intramolecular Mitsunobu cyclization of the carbinols, manipulation of the protecting groups, and subsequent ring closure to result in the formation of 7-amino-3-(β-d-ribofuranosyl)pyrazolo[4,3-b]pyridine. Georg Thieme Verlag Stuttgart.
Selective deoxygenation of heteroaromatic N-oxides with olefins catalyzed by ruthenium porphyrin
Nakagawa, Hiroshi,Higuchi, Tsunehiko,Kikuchi, Kazuya,Urano, Yasuteru,Nagano, Tetsuo
, p. 1656 - 1657 (2007/10/03)
A new convenient method of deoxygenation of heteroaromatic N-oxides is described. Ruthenium porphyrin was used as a catalyst and this method expressed high yields for o-substituted pyridine N-oxides, quinoline N-oxide derivatives, acridine N-oxide, etc. under mild conditions. Moreover, nitro-, benzyloxy-, and ketone carbonyl groups, which can be affected by the usual deoxygenation methods such as catalytic hydrogenation or borane reduction, were retained.
8-Arylalkyl- and 8-arylheteroalkyl-5, 11-dihydro-6H-dipyrido-[3,2-b:2', 3'-e][1,4]diazepines and their use in the prevention or treatment of HIV infection
-
, (2008/06/13)
The invention relates to novel 8-arylalkyl-5,11-dihydro-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepines of general formula 1 which are useful in the prevention or treatment of HIV infection.
