135264-36-7 Usage
Uses
Used in Pharmaceutical Research:
(5-(nitro-2-furyl)-1,3,4-oxadiazol-2-ylthio)acethydrazide is used as a compound in pharmaceutical research for its potential biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Its unique structure and pharmacological properties make it an important candidate for the development of new drugs and therapies.
Used in Organic Synthesis:
(5-(nitro-2-furyl)-1,3,4-oxadiazol-2-ylthio)acethydrazide is used as a building block in organic synthesis, allowing for the creation of various complex molecules with potential applications in different industries.
Used in Chemical and Biological Systems:
(5-(nitro-2-furyl)-1,3,4-oxadiazol-2-ylthio)acethydrazide is used as a fluorescent probe for the detection of metal ions in chemical and biological systems, providing valuable insights into the interactions between metal ions and other molecules.
Used in Drug Development:
(5-(nitro-2-furyl)-1,3,4-oxadiazol-2-ylthio)acethydrazide is used as a starting material in drug development, with its potential applications in the creation of new pharmaceuticals targeting various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 135264-36-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,2,6 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 135264-36:
(8*1)+(7*3)+(6*5)+(5*2)+(4*6)+(3*4)+(2*3)+(1*6)=117
117 % 10 = 7
So 135264-36-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N5O5S/c9-10-5(14)3-19-8-12-11-7(18-8)6-4(13(15)16)1-2-17-6/h1-2H,3,9H2,(H,10,14)
135264-36-7Relevant academic research and scientific papers
Antituberculosis agents. V: α-[5-(5-Nitro-2-furyl)-1,3,4-oxadiazol-2-ylthio]acethydrazide and related compounds
Mir,Siddiqui,Comrie
, p. 548 - 550 (2007/10/02)
α-[5-(5-Nitro-2-furyl)-1,3,4-oxadiazol-2-ylthio]acethydrazide, α-[5-(5-nitro-2-furyl)-1,3,4-oxadiazol-2-ylthio]acetamide, δ-allyl-1-([5-(5-nitro-2-furyl)-1,3,4-oxadiazol-2-ylthio]acety) thiosemicarbazide, and other related compounds have been synthesised
