40017-65-0 Usage
Description
7-Bromo-5-(2-chlorophenyl)-1,3-dihydro-2H-thieno(2,3-e)(1,4)diazepin-2-one is a heterocyclic organic compound with the molecular formula C14H9BrClN2OS. It features a thieno-diazepine ring structure, a bromine atom, a chlorophenyl group, and a thieno-diazepinone core. 7-Bromo-5-(2-chlorophenyl)-1,3-dihydro-2H-thieno(2,3-e)(1,4)diazepin-2-one is often utilized in pharmaceutical research and drug development due to its potential therapeutic applications and biological activity.
Uses
Used in Pharmaceutical Research and Drug Development:
7-Bromo-5-(2-chlorophenyl)-1,3-dihydro-2H-thieno(2,3-e)(1,4)diazepin-2-one is used as a potential therapeutic agent in pharmaceutical research and drug development. Its unique structure and biological activity make it a promising candidate for the development of new medications.
Used in Medicinal Chemistry and Drug Discovery:
In the field of medicinal chemistry and drug discovery, 7-Bromo-5-(2-chlorophenyl)-1,3-dihydro-2H-thieno(2,3-e)(1,4)diazepin-2-one is used for its potential anti-inflammatory and anti-cancer activities. Studies have shown that this compound may have significant effects on these therapeutic areas, warranting further investigation and development.
Used in Anti-Inflammatory Applications:
7-Bromo-5-(2-chlorophenyl)-1,3-dihydro-2H-thieno(2,3-e)(1,4)diazepin-2-one is used as an anti-inflammatory agent. Its structure and properties suggest that it may help in reducing inflammation, which is a key factor in various diseases and conditions.
Used in Anti-Cancer Applications:
7-Bromo-5-(2-chlorophenyl)-1,3-dihydro-2H-thieno(2,3-e)(1,4)diazepin-2-one is also used as an anti-cancer agent. Its potential to exhibit anti-tumor activity makes it a valuable compound in the search for new cancer treatments.
Used in Chemical Synthesis:
In the chemical synthesis industry, 7-Bromo-5-(2-chlorophenyl)-1,3-dihydro-2H-thieno(2,3-e)(1,4)diazepin-2-one may be used as a starting material or intermediate in the synthesis of other complex organic compounds, particularly those with potential pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 40017-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,0,1 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40017-65:
(7*4)+(6*0)+(5*0)+(4*1)+(3*7)+(2*6)+(1*5)=70
70 % 10 = 0
So 40017-65-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H8BrClN2OS/c14-10-5-8-12(7-3-1-2-4-9(7)15)16-6-11(18)17-13(8)19-10/h1-5,16H,6H2
40017-65-0Relevant articles and documents
Process for preparing 6-aryl-4H-S-triazolo[3,4-c]-thieno[2,3-e]-1,4-diazepines
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, (2008/06/13)
An improved process for preparing 6-aryl-4H-s-triazolo[3,4-c]-thieno[2,3-e]-1,4-diazepines of formula I, wherein: R1 is a hydrogen or halogen atom or a C1-C6 alkyl group, R2 is a hydrogen or halogen atom or a C1-C6 alkyl, C1-C6 hydroxyalkyl, C3-C6 cycloalkyl group or a 5- or 6-membered oxygen-, sulphur- or nitrogen-containing heterocyclic group which may optionally be substituted at the nitrogen atom by a C1-C3 alkyl group, and R3 is a hydrogen or halogen atom,
