4,5,6,7-Tetrahydro-1-benzothiophene-3-carboxylic acid

• CAS: 19156-54-8
• Catalog Number: ACM19156548
• Category: Other Products
• Molecular Weight: 182.24
• Molecular Formula: C9H10O2S
• Synonyms: ZINC00245897, CID3634058, 19156-54-8
• IUPAC Name: 4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate
• InChI Key: TUZZQEHPGHKGRJ-UHFFFAOYSA-M
• Boiling Point: 350.5ºC at 760mmHg
• Flash Point: 165.8ºC
• Density: 1.317g/cm³
• Exact Mass: 182.04000
• H-Bond Acceptor: 2
• H-Bond Donor: 0

Synthetic Use

Upstream Synthesis Route 1

• 14559-12-7

• 19156-54-8

Reference: [1] Journal of Medicinal Chemistry, 2003, vol. 46, # 12, p. 2446 - 2455
[2] Chemistry of Heterocyclic Compounds, 2015, vol. 50, # 12, p. 1748 - 1755[3] Khim. Geterotsikl. Soedin., 2014, vol. 50, # 12, p. 1900 - 1907,8

Upstream Synthesis Route 2

• 4506-71-2

• 19156-54-8

Reference: [1] Journal of Medicinal Chemistry, 2003, vol. 46, # 12, p. 2446 - 2455
[2] Chemistry of Heterocyclic Compounds, 2015, vol. 50, # 12, p. 1748 - 1755[3] Khim. Geterotsikl. Soedin., 2014, vol. 50, # 12, p. 1900 - 1907,8

Upstream Synthesis Route 3

• 14559-12-7

• 19156-54-8

Reference: [1]Journal of Medicinal Chemistry,2003,vol. 46,p. 2446 - 2455
[2]Chemistry of Heterocyclic Compounds,2015,vol. 50,p. 1748 - 1755
Khim. Geterotsikl. Soedin.,2014,vol. 50,p. 1900 - 1907,8

Upstream Synthesis Route 4

• 4506-71-2

• 19156-54-8

Reference: [1]Journal of Medicinal Chemistry,2003,vol. 46,p. 2446 - 2455
[2]Chemistry of Heterocyclic Compounds,2015,vol. 50,p. 1748 - 1755
Khim. Geterotsikl. Soedin.,2014,vol. 50,p. 1900 - 1907,8

Downstream Synthesis Route 1

• 19156-54-8

• 851634-59-8

Reference: [1]Patent: JP2016/222570,2016,A .Location in patent: Paragraph 0061

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