alpha-Terthienylmethanol structure, CAS 13059-93-3

alpha-Terthienylmethanol

CAS Number13059-93-3

Synonyms2,2':5',2''-Terthien-5-ylmethanol; 2,2':5',2''-Terthiophen-5-ylmethanol; [2,2':5',2''-Terthiophene]-5-methanol

Molecular FormulaC13H10OS3

Molecular Weight278.41

Purity

Density1.4±0.1 g/cm3

Boiling Point424.7±40.0 °C at 760 mmHg

Melting Point

Flash Point

Appearanceyellow powder

EINECS

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Symbol

Signal Word

Cat. No.: 2A-9068346 Purity:
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Chemical & Physical Properties
CAS Number13059-93-3
Catalog No.2A-9068346
Chinese Nameα-三联噻吩甲醇
Synonyms2,2':5',2''-Terthien-5-ylmethanol; 2,2':5',2''-Terthiophen-5-ylmethanol; [2,2':5',2''-Terthiophene]-5-methanol
Molecular FormulaC13H10OS3
Molecular Weight278.41
Density1.4±0.1 g/cm3
Boiling Point424.7±40.0 °C at 760 mmHg
Appearanceyellow powder
Storage Conditionroom temperature
Applicationα-Terthienylmethanol is a terthiophene isolated from the n-hexane fraction of E. prostrata. α-Terthienylmethanol has potent cytotoxic activity (IC50 < 1 μM) against human endometrial cancer cells (Hec
HTC2934999090
SMILESOCc1ccc(-c2ccc(-c3cccs3)s2)s1
InChI KeyWAYZWWNNJZMQCQ-UHFFFAOYSA-N
Use ofα-Terthienylmethanol is a terthiophene isolated from the n-hexane fraction of E. prostrata. α-Terthienylmethanol has potent cytotoxic activity against human endometrial cancer cells (Hec1A and Ishikawa) (IC50 < 1 μM). α-Terthienylmethanol increases the intracellular level of ROS and decreases that of GSH[1]. Properties Name [5-(5-thiophen-2-ylthiophen-2-yl)thiophen-2-yl]methanol Synonym More Synonyms 2,2':5',2''-Terthien-5-ylmethanol Biological Activity Description α-Terthienylmethanol is a terthiophene isolated from the n-hexane fraction of E. prostrata. α-Terthienylmethanol has potent cytotoxic activity against human endometrial cancer cells (Hec1A and Ishikawa) (IC50 < 1 μM). α-Terthienylmethanol increases the intracellular level of ROS and decreases that of GSH[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Jae-Seung Lee, et al. α-Terthienylmethanol, isolated from Eclipta prostrata, induces apoptosis by generating reactive oxygen species via NADPH oxidase in human endometrial cancer cells. J Ethnopharmacol. 2015, 169. Chemical & Physical Properties Molecular Formula C13H10OS3 Exact Mass 277.989380 PSA 104.95000 Index of Refraction 1.687 InChIKey WAYZWWNNJZMQCQ-UHFFFAOYSA-N Safety Information HS Code 2934999090
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport InfoProduct name: Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
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