Cas no 21175-51-9 (2-(5-bromothiophen-2-yl)-2-oxoacetaldehyde hydrate)

2-(5-Bromothiophen-2-yl)-2-oxoacetaldehyde hydrate is a brominated thiophene derivative featuring a reactive α-ketoaldehyde functionality. This compound is particularly valuable in synthetic organic chemistry as a versatile intermediate for constructing heterocyclic frameworks, pharmaceuticals, and functional materials. The presence of both an aldehyde and a ketone group enables diverse reactivity, including nucleophilic additions and condensation reactions, while the bromine substituent facilitates further functionalization via cross-coupling methodologies. The hydrate form enhances stability and handling, making it suitable for controlled synthetic applications. Its structural features make it a useful precursor in the development of bioactive molecules and advanced materials, particularly in medicinal and materials chemistry research.
2-(5-bromothiophen-2-yl)-2-oxoacetaldehyde hydrate structure
21175-51-9 structure
Product Name:2-(5-bromothiophen-2-yl)-2-oxoacetaldehyde hydrate
CAS No:21175-51-9
MF:C6H5BrO3S
MW:237.071099996567
CID:911255
PubChem ID:44118546
Update Time:2025-10-19

2-(5-bromothiophen-2-yl)-2-oxoacetaldehyde hydrate Chemical and Physical Properties

Names and Identifiers

    • 2-(5-bromothiophen-2-yl)-2-oxoacetaldehyde hydrate
    • 2-(5-bromothiophen-2-yl)-2-oxoacetaldehydehydrate
    • AKOS015935072
    • DS-3509
    • (5-Bromothiophen-2-yl)(oxo)acetaldehyde--water (1/1)
    • 1170045-14-3
    • 2-(5-bromothiophen-2-yl)-2-oxoacetaldehyde;hydrate
    • DTXSID30656872
    • J-013902
    • (5-Bromothien-2-yl)glyoxal hydrate
    • 21175-51-9
    • AB48670
    • Inchi: 1S/C6H3BrO2S.H2O/c7-6-2-1-5(10-6)4(9)3-8;/h1-3H;1H2
    • InChI Key: FEJAPSSZHPASMZ-UHFFFAOYSA-N
    • SMILES: BrC1=CC=C(C(C=O)=O)S1.O

Computed Properties

  • Exact Mass: 235.91428g/mol
  • Monoisotopic Mass: 235.91428g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 160
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 63.4?2

2-(5-bromothiophen-2-yl)-2-oxoacetaldehyde hydrate Pricemore >>

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2-(5-bromothiophen-2-yl)-2-oxoacetaldehyde hydrate Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Selenium dioxide ,  Water Solvents: 1,4-Dioxane ;  5 h, 80 °C
Reference
Substrate-Controlled Three-Component Synthesis of Diverse Fused Heterocycles
Peshkov, Anatoly A.; Gapanenok, Diana; Puzyk, Aleksandra; Amire, Niyaz; Novikov, Alexander S. ; et al, Journal of Organic Chemistry, 2023, 88(15), 10508-10524

2-(5-bromothiophen-2-yl)-2-oxoacetaldehyde hydrate Raw materials

2-(5-bromothiophen-2-yl)-2-oxoacetaldehyde hydrate Preparation Products

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