38185-56-7 Usage
Uses
Used in Pharmaceutical Industry:
2-Fluoro-3-Chloro-5-Bromopyridine is used as a building block for the synthesis of pharmaceuticals. Its unique combination of halogen atoms allows for the creation of more complex molecular structures, which can be further modified to develop new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
2-Fluoro-3-Chloro-5-Bromopyridine is used as a precursor in the synthesis of agrochemicals. Its reactivity and stability can be leveraged to develop new compounds with improved efficacy and selectivity in pest control and crop protection.
Used in Organic Synthesis:
2-Fluoro-3-Chloro-5-Bromopyridine is used as a versatile intermediate in organic synthesis. Its presence of halogen atoms can be utilized for various chemical reactions, such as cross-coupling, nucleophilic substitution, and electrophilic aromatic substitution, to form a wide range of organic compounds with diverse applications.
Further research and experimentation with 2-Fluoro-3-Chloro-5-Bromopyridine may reveal additional applications and uses for this chemical, expanding its potential in various industries and scientific fields.
Check Digit Verification of cas no
The CAS Registry Mumber 38185-56-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,8 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38185-56:
(7*3)+(6*8)+(5*1)+(4*8)+(3*5)+(2*5)+(1*6)=137
137 % 10 = 7
So 38185-56-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H2BrClFN/c6-3-1-4(7)5(8)9-2-3/h1-2H
38185-56-7Relevant academic research and scientific papers
HETEROARYLOXY QUINAZOLINE DERIVATIVE
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Page/Page column 46, (2010/09/05)
Disclosed are compounds of the following formula and their pharmaceutically-acceptable salts, which have an effect of glucokinase activation and are useful in the field of medicines for treatment for diabetes, obesity, etc. (wherein ring A represents a pyrazolyl group optionally having a lower alkyl group, etc.; ring B represents a heteroaryl group; R represents a lower alkyl group, etc.; R1 represents a group of a formula: (wherein R11 and R12 each independently represent a hydrogen atom, etc.; m indicates an integer of from 2 to 6), etc.; R2 represents a lower alkyl group, etc.; r indicates an integer of from 0 to 3; k indicates an integer of from 0 to 4).
FLUOROISOQUINOLINE SUBSTITUTED THIAZOLE COMPOUNDS AND METHODS OF USE
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Page/Page column 143-144, (2010/08/08)
The invention relates to thiazole compounds of Formula (I) and compositions thereof useful for treating diseases mediated by protein kinase B (PKB) where the variables have the definitions provided herein. The invention also relates to the therapeutic use of such thiazole compounds and compositions thereof in treating disease states associated with abnormal cell growth, cancer, inflammation, and metabolic disorders.