25109-26-6 Usage
Uses
Used in Organic Synthesis:
2-Selenophenecarboxaldehyde (6CI,7CI,8CI,9CI) is utilized as a key building block in the preparation of various organic compounds. Its reactivity and the presence of the selenophene ring make it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-Selenophenecarboxaldehyde (6CI,7CI,8CI,9CI) is employed for its potential applications in the development of new pharmaceuticals. The selenophene ring and carboxaldehyde group can be exploited to create novel drug candidates with unique biological activities.
Used in Materials Science:
2-Selenophenecarboxaldehyde (6CI,7CI,8CI,9CI) also finds use in materials science, where its properties can be harnessed to develop new materials with specific characteristics. The selenophene ring's electronic and structural features contribute to the creation of materials with tailored properties for various applications.
Used as a Reagent in Chemical Reactions:
Furthermore, 2-Selenophenecarboxaldehyde (6CI,7CI,8CI,9CI) serves as a reagent in various chemical reactions, facilitating the synthesis of target compounds and enabling specific transformations that are otherwise challenging to achieve. Its reactivity and stability make it a useful tool in the hands of chemists.
Check Digit Verification of cas no
The CAS Registry Mumber 25109-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,0 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25109-26:
(7*2)+(6*5)+(5*1)+(4*0)+(3*9)+(2*2)+(1*6)=86
86 % 10 = 6
So 25109-26-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H4OSe/c6-4-5-2-1-3-7-5/h1-4H
25109-26-6Relevant articles and documents
THE ACTION OF THIOLS ON DERIVATIVES OF D-XYLOSE
Blumberg, Karl,Es, Theodorus van
, p. 253 - 266 (2007/10/02)
The action of thiols on 1,2,3,4-tetra-O-acetyl β-D-xylopyranose gave 2- and 5-alkylthiopentose dithioacetals and alkyl 1-thio-D-xylopyranosides.On treatment with thiols and trifluoroacetic acid, 3-O-acetyl-1,2-O-isopropylidene-α-D-xylofuranose derivatives rapidly formed 4-O-acetyl-2,3-dialkylthio-D-ribose dithioacetal derivatives, which were in turn converted into 4-O-acetyl-3-S-benzyl-2,5-epithio-3-thio-D-ribose (or D-arabinose) dithioacetal.
