592862
3-氯苯并[b]噻吩-2-羧酸
97%
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经验公式（希尔记法）:
C9H5ClO2S
化学文摘社编号:
分子量:
212.65
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
3-氯苯并[b]噻吩-2-羧酸, 97%
InChI
1S/C9H5ClO2S/c10-7-5-3-1-2-4-6(5)13-8(7)9(11)12/h1-4H,(H,11,12)
SMILES string
OC(=O)c1sc2ccccc2c1Cl
InChI key
HJTMIYKPPPYDRJ-UHFFFAOYSA-N
assay
97%
form
solid
mp
268-272 °C (lit.)
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Application
3-Chloro-benzo[b]thiophene-2-carboxylic acid may be used in the synthesis of the following:
- 5-(3-chlorobenzo[b]thiophen-2-yl)-1,3,4-thiadiazol-2-ylamine via condensation with thiosemicarbazide in the presence of POCl3
- 2-benzo[b]thiophen-2-yl-6-methylbenzo[d][1;3]oxazi-4-one via reaction with 2-amino-5-methyl-benzoic acid in the presence of carbonyl diimidazole
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Neutral Inhibitors of the Serine Protease Factor Xa?
Shrader.DW, et al.
Bioorganic & Medicinal Chemistry Letters, 11(14), 1801- 1804 (2001)
Synthesis and biological activity of new 1,3,4-thiadiazole derivatives?
Aly.A.A and Sayed-LE.R
Chemical Papers, 60(01), 56-60 (2006)
Michael D Neinast et al.
Cell metabolism, 29(2), 417-429 (2018-11-20)
Elevations in branched-chain amino acids (BCAAs) associate with numerous systemic diseases, including cancer, diabetes, and heart failure. However, an integrated understanding of whole-body BCAA metabolism remains lacking. Here, we employ in vivo isotopic tracing to systemically quantify BCAA oxidation in healthy
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