跳转至内容
Merck
CN

91095

Sigma-Aldrich

三氯乙酰异氰酸酯

purum, ≥97.0% (GC)

别名:

2,2,2-Trichloroacetyl isocyanate, alpha,alpha,alpha-Trichloroacetyl isocyanate

登录查看公司和协议定价


About This Item

线性分子式:
Cl3CCONCO
CAS号:
分子量:
188.40
Beilstein:
971201
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

等级

purum

质量水平

检测方案

≥97.0% (GC)

形式

liquid

折射率

n20/D 1.480 (lit.)
n20/D 1.480

bp

80-85 °C/20 mmHg (lit.)

密度

1.581 g/mL at 25 °C (lit.)

储存温度

2-8°C

SMILES字符串

ClC(Cl)(Cl)C(=O)N=C=O

InChI

1S/C3Cl3NO2/c4-3(5,6)2(9)7-1-8

InChI key

GRNOZCCBOFGDCL-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

一般描述

Trichloroacetyl isocyanate (TAI) is a versatile building block in organic synthesis. It is also used as an in situ derivatizing reagent for the characterization of phenols, alcohols, and amines.

应用


  • One-pot synthesis of 2-acylaminobenzimidazoles: A study on the synthesis of 2-acylaminobenzimidazoles via a reaction between trichloroacetyl isocyanate and 1,2-phenylenediamine derivatives (Shajari et al., 2018).

  • Cabamothioate compounds: Research on the synthesis of S-aryl (trichloroacetyl) carbamothioate from a reaction of 2-naphthalenethiol or thiophenol derivatives and trichloroacetyl isocyanate (Shajari et al., 2021).

  • Chiral calyx[4]arenes: Diastereoselective synthesis of inherently chiral calyx[4]arenes via reaction of trichloroacetyl isocyanate with 1,3-dihydroxy calixarene (Boyko et al., 2016).

其他说明

衍生化试剂,用于通过 NMR 测定羟基化合物的结构;用于负离子化学电离质谱

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

闪点(°F)

150.8 °F - closed cup

闪点(°C)

66 °C - closed cup

个人防护装备

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


Choose from one of the most recent versions:

分析证书(COA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

If you need assistance, please contact 客户支持

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

H. Fujiwara et al.
Pract. Spectrosc., 3, 329-329 (1980)
Determination of chain branching in epoxy resins by nuclear magnetic resonance spectrometry.
H D Mak et al.
Analytical chemistry, 44(4), 837-839 (1972-04-01)
D.R. Taylor
Canadian Journal of Chemistry, 54, 189-189 (1976)
M. Budesinsky et al.
Collection of Czechoslovak Chemical Communications, 45, 2784-2784 (1980)
Ian Paterson et al.
Angewandte Chemie (International ed. in English), 53(10), 2692-2695 (2014-02-01)
Leiodermatolide is an antimitotic macrolide isolated from the marine sponge Leiodermatium sp. whose potentially novel tubulin-targeting mechanism of action makes it an exciting lead for anticancer drug discovery. In pursuit of a sustainable supply, we report a highly stereocontrolled total

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