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Merck
CN

T15601

四氢噻吩

99%

别名:

THT, 噻吩烷, 四氢硫杂茂, 四甲撑硫

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关于此项目

经验公式(希尔记法):
C4H8S
化学文摘社编号:
分子量:
88.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-728-9
Beilstein/REAXYS Number:
102392
MDL number:
Assay:
99%
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InChI key

RAOIDOHSFRTOEL-UHFFFAOYSA-N

InChI

1S/C4H8S/c1-2-4-5-3-1/h1-4H2

SMILES string

C1CCSC1

vapor pressure

18 mmHg ( 25 °C)

assay

99%

refractive index

n20/D 1.504 (lit.)

bp

119 °C (lit.)

mp

−96 °C (lit.)

density

1 g/mL at 25 °C (lit.)

Quality Level

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Application

四氢噻吩可用作合成各种环氧化物及其衍生物的试剂。它可用作合成苯并[n.1.0]双环烷烃的催化剂。

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

55.4 °F - closed cup

flash_point_c

13 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo-and enantioselectivities.
Aggarwal VK, et al.
Journal of the American Chemical Society, 125(36), 10926-10940 (2003)
Catalytic asymmetric synthesis of epoxides from aldehydes using sulfur ylides with in situ generation of diazocompounds.
Aggarwal VK, et al.
Angewandte Chemie (International Edition in English), 40(8), 1430-1433 (2001)
Tetrahydrothiophene-catalyzed synthesis of benzo [n.1.0] bicycloalkanes.
Ye LW, et al.
The Journal of Organic Chemistry, 72(4), 1335-1340 (2007)
Benoit Gautier et al.
Chemistry & biology, 18(12), 1631-1639 (2011-12-27)
Protein-protein interactions play a central role in medicine, and their modulation with small organic compounds remains an enormous challenge. Because it has been noted that the macromolecular complexes modulated to date have a relatively pronounced binding cavity at the interface
V I Smol'iakova et al.
Eksperimental'naia i klinicheskaia farmakologiia, 74(8), 37-40 (2012-01-12)
A hepatoprotective effect of thiophan was studied on the model of carbon tetrachloride-induced hepatitis in rats. Therapeutic administration of thiophan repairs the antitoxic function of liver, normalizes cytolysis marker activity, and improves the synthetic function of liver and the carbohydrate

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