2,5-Thiophenedicarboxaldehyde

• CAS: 932-95-6
• Catalog Number: ACM932956
• Category: Other Products
• Molecular Weight: 140.16
• Molecular Formula: C6H4O2S
• Synonyms: Thiophene-2,5-dialdehyde
• IUPAC Name: thiophene-2,5-dicarbaldehyde
• Canonical SMILES: C1=C(SC(=C1)C=O)C=O
• InChI: InChI=1S/C6H4O2S/c7-3-5-1-2-6(4-8)9-5/h1-4H
• InChI Key: OTMRXENQDSQACG-UHFFFAOYSA-N
• Boiling Point: 226.66 ºC
• Melting Point: 115-117 ºC (lit.)
• Density: 1.327 g/ml

Custom Q&A

What is the molecular formula of 2,5-Thiophenedicarboxaldehyde?

The molecular formula of 2,5-Thiophenedicarboxaldehyde is C6H4O2S.

What is the molecular weight of 2,5-Thiophenedicarboxaldehyde?

The molecular weight of 2,5-Thiophenedicarboxaldehyde is 140.16 g/mol.

What is the IUPAC name of 2,5-Thiophenedicarboxaldehyde?

The IUPAC name of 2,5-Thiophenedicarboxaldehyde is thiophene-2,5-dicarbaldehyde.

What is the InChI of 2,5-Thiophenedicarboxaldehyde?

The InChI of 2,5-Thiophenedicarboxaldehyde is InChI=1S/C6H4O2S/c7-3-5-1-2-6(4-8)9-5/h1-4H.

What is the InChIKey of 2,5-Thiophenedicarboxaldehyde?

The InChIKey of 2,5-Thiophenedicarboxaldehyde is OTMRXENQDSQACG-UHFFFAOYSA-N.

What is the canonical SMILES of 2,5-Thiophenedicarboxaldehyde?

The canonical SMILES of 2,5-Thiophenedicarboxaldehyde is C1=C(SC(=C1)C=O)C=O.

What is the CAS number of 2,5-Thiophenedicarboxaldehyde?

The CAS number of 2,5-Thiophenedicarboxaldehyde is 932-95-6.

What is the EC number of 2,5-Thiophenedicarboxaldehyde?

The EC number of 2,5-Thiophenedicarboxaldehyde is 627-004-0.

What is the ChEMBL ID of 2,5-Thiophenedicarboxaldehyde?

The ChEMBL ID of 2,5-Thiophenedicarboxaldehyde is CHEMBL2229528.

Synthetic Use

Upstream Synthesis Route 1

• 3141-27-3
• 121-43-7

• 188290-36-0
• 932-95-6
• 26076-46-0

Reference: [1] New Journal of Chemistry, 2002, vol. 26, # 4, p. 373 - 375

Upstream Synthesis Route 2

• 3141-27-3
• 68-12-2

• 932-95-6

Reference: [1] Chemistry of Materials, 2014, vol. 26, # 24, p. 7229 - 7235
[2] Tetrahedron Letters, 2013, vol. 54, # 22, p. 2795 - 2798
[3] Organic Letters, 2012, vol. 14, # 1, p. 78 - 81
[4] Journal of the American Chemical Society, 1995, vol. 117, # 9, p. 2467 - 2478

Upstream Synthesis Route 3

• 110-02-1
• 68-12-2

• 932-95-6

Reference: [1]Bromby, Ashley D.; Keller, Samantha N.; Bozek, Kevin J. A.; Williams, Vance E.; Sutherland, Todd C.
[Journal of Organic Chemistry, 2015, vol. 80, # 19, p. 9401 - 9409]

Upstream Synthesis Route 4

• 3141-27-3
• 68-12-2

• 932-95-6

Reference: [1]Kawano, Tomikazu; Matsumoto, Naomi; Nakanishi-Matsui, Mayumi; Ogawa, Satoshi; Ohashi, Toshika; Sugawara, Aoi; Tamura, Satoru
[Heterocycles, 2020, vol. 100, # 8, p. 1233 - 1247]

Downstream Synthesis Route 1

• 932-95-6

• 4565-31-5

Reference: [1] Beilstein Journal of Organic Chemistry, 2013, vol. 9, p. 602 - 607

Downstream Synthesis Route 2

• 932-95-6

• 6007-86-9

Reference: [1]Dong, Yixin; Ji, Xiaofei; Liu, Yongsheng; Lu, Di; Lv, Guangwei; Xu, Zhiyuan
[Journal of the American Chemical Society, 2020, vol. 142, # 25, p. 11114 - 11122]

* For details of the synthesis route, please refer to the original source to ensure accuracy.