22353-38-4 Usage
Uses
Used in Pharmaceutical Industry:
3-CHLORO-2-HYDROXY-5-NITROPYRIDINE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 3-CHLORO-2-HYDROXY-5-NITROPYRIDINE serves as an intermediate in the production of agrochemicals. Its reactive nature enables it to be incorporated into the synthesis of compounds that can be used in pest control and crop protection, thereby supporting agricultural productivity.
Used in Organic Chemistry Research:
3-CHLORO-2-HYDROXY-5-NITROPYRIDINE is utilized as a molecular building block in organic chemistry. Its presence of functional groups such as the nitro and chloro groups makes it a valuable compound for exploring new reaction pathways and developing innovative synthetic methods in organic chemistry research.
Check Digit Verification of cas no
The CAS Registry Mumber 22353-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,5 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22353-38:
(7*2)+(6*2)+(5*3)+(4*5)+(3*3)+(2*3)+(1*8)=84
84 % 10 = 4
So 22353-38-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H6ClNO/c1-4-2-5(7)6(9)8-3-4/h2-3H,1H3,(H,8,9)
22353-38-4Relevant academic research and scientific papers
Facile entry into structurally diverse, privileged, (hetero)arene-fused N-alkoxy 3,4-dihydrobenzo[f][1,4]oxazepin-5(2H)-ones
Sapegin, Alexander,Reutskaya, Elena,Smirnov, Alexey,Korsakov, Mikhail,Krasavin, Mikhail
supporting information, p. 5877 - 5880 (2016/12/14)
Rare and highly medicinally relevant N-alkoxy-substituted benzo[1,4]oxazepines have been synthesized conveniently via the base-promoted SNAr/Smiles rearrangement/SNAr tandem cyclization of N-alkoxysalicylamides with a range of bis-electrophilic substrates; subsequent de-alkylation gives rise to the respective N-hydroxy versions. The compounds reported herein significantly add to the contemporary arsenal of small molecule tools for drug discovery.
