跳转至内容
Merck

T15601

Sigma-Aldrich

四氢噻吩

99%

别名:

THT, 噻吩烷, 四氢硫杂茂, 四甲撑硫

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
C4H8S
CAS号:
分子量:
88.17
Beilstein:
102392
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

蒸汽壓力

18 mmHg ( 25 °C)

品質等級

化驗

99%

折射率

n20/D 1.504 (lit.)

bp

119 °C (lit.)

mp

−96 °C (lit.)

密度

1 g/mL at 25 °C (lit.)

SMILES 字串

C1CCSC1

InChI

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

InChI 密鑰

RAOIDOHSFRTOEL-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

應用

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。

象形圖

FlameExclamation mark

訊號詞

Danger

危險分類

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

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

55.4 °F - closed cup

閃點(°C)

13 °C - closed cup

個人防護裝備

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


从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

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)
Tetrahydrothiophene-catalyzed synthesis of benzo [n.1.0] bicycloalkanes.
Ye LW, et al.
The Journal of Organic Chemistry, 72(4), 1335-1340 (2007)
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)
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
James C Ritchie et al.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 28(1), 22-33 (2002-12-24)
Using purified enzyme preparations, we investigated the actions of angiotensin-converting enzyme, aminopeptidase N, and endopeptidase 24.11 on corticotropin-releasing factor (CRF). The effects of inhibition of these enzymes on CRF action in rat anterior pituitary cultures were also determined. Finally, specific

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门