5370-19-4 Usage
Description
5-Iodothiophene-2-carbaldehyde is a chemical compound with the molecular formula C6H4IO. It is a derivative of thiophene, a heterocyclic compound containing a five-membered ring of four carbon atoms and one sulfur atom. The presence of the iodine and aldehyde functional groups in this compound make it useful in a variety of organic synthesis reactions.
Used in Pharmaceutical Industry:
5-Iodothiophene-2-carbaldehyde is used as a building block for the synthesis of pharmaceuticals due to its unique chemical structure and reactivity.
Used in Agrochemical Industry:
5-Iodothiophene-2-carbaldehyde is used as a building block for the synthesis of agrochemicals, contributing to the development of new and effective pesticides and other agricultural chemicals.
Used in Electronic Materials Industry:
5-Iodothiophene-2-carbaldehyde is used as a building block for the synthesis of materials for electronic applications, such as organic semiconductors and other components in electronic devices.
Used in Antiviral Applications:
5-Iodothiophene-2-carbaldehyde and its derivatives have been investigated for their antiviral properties, making them potential candidates for the development of new antiviral drugs.
Used in Antibacterial Applications:
5-Iodothiophene-2-carbaldehyde and its derivatives have shown potential antibacterial activity, indicating their potential use in the development of new antibiotics.
Used in Anti-inflammatory Applications:
5-Iodothiophene-2-carbaldehyde and its derivatives have been studied for their anti-inflammatory properties, suggesting their potential use in the development of new anti-inflammatory drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 5370-19-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,7 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5370-19:
(6*5)+(5*3)+(4*7)+(3*0)+(2*1)+(1*9)=84
84 % 10 = 4
So 5370-19-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H3IOS/c6-5-2-1-4(3-7)8-5/h1-3H
5370-19-4Relevant articles and documents
METHOD FOR PRODUCING CARBONYL COMPOUND
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Paragraph 0032-0035, (2018/03/23)
PROBLEM TO BE SOLVED: To provide a method for producing a carbonyl compound, allowing for improvement of ease of production and furthermore allowing for reduction of production cost, by positively utilizing inexpensive iodine. SOLUTION: A carbonyl compound is produced by mixing primary alcohol or secondary alcohol, and iodic acid (HIO3) in a non-solvent or an aprotic polar solvent based on the following general formula (1), where R1 is an optionally substituted linear- or branched 1-12C aliphatic group, or an optionally substituted aromatic group; R2 is a hydrogen atom, an optionally substituted linear- or branched 1-12C alkyl group, or an optionally substituted aromatic group; R1 and R2 each may be coupled with each other to form a ring of aromatic group or a non-aromatic group. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT
Chemistry of polyhalogenated nitrobutadienes, part 11: Ipso-formylation of 2-chlorothiophenes under Vilsmeier-Haack conditions
Vogt, Eva-Janina,Zapol'skii, Viktor A.,Nutz, Eva,Kaufmann, Dieter E.
experimental part, p. 285 - 294 (2012/07/14)
The regioselective ipso-formylation of electron-rich, 3,4-push-pull- substituted 2-chlorothiophenes under Vilsmeier-Haack conditions was performed in good yields. The synthetic scope of this new reaction was explored using various halothiophenes, chloroanilines, and 1-methyl-3-chloroindole. In comparison with their structural C-H analogs the chlorinated thiophenes, anilines, and the indole proved to be less reactive toward electrophilic attack by chloromethyleniminium salts.