跳转至内容
Merck
所有图片(1)

Key Documents

View All Documentation

518352

Sigma-Aldrich

2-羟甲基-3,4-二氢吡喃，聚合物键合型

extent of labeling: ~0.7 mmol/g loading, 1 % cross-linked

别名:

DHP 树脂, Ellmans DHP 树脂

登录查看公司和协议定价
所有图片(1)

About This Item

MDL號碼:
MFCD01321550
分類程式碼代碼:
12352202
PubChem物質ID:
24874015
NACRES:
NA.22

交聯

1 % cross-linked

反應適用性

reaction type: Fmoc solid-phase peptide synthesis
reactivity: alcohol reactive

標籤範圍

~0.7 mmol/g loading

SMILES 字串

C=Cc1ccccc1.C=Cc2ccc(C=C)cc2.C3CC(COCc4ccccc4)OC=C3

相关类别

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ （Lot或Batch）字后找到。

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

相关内容

Ellman Group – Professor Product Portal

The Ellman group has participated in the development of a variety of C-H functionalization methods. An electron rich phosphine ligand has proven to be very useful for a variety of Rh(I)-catalyzed C-C bond forming reactions applicable to heterocycle synthesis as exemplified in the recent Science paper “Proton Donor Acidity Controls Selectivity in Nonaromatic Nitrogen Heterocycle Synthesis.” Another useful ligand developed for the highly functional group compatible direct arylation of nitrogen heterocycles is described in a 2008 J. Am. Chem. Soc. paper “Rh(I)-Catalyzed Arylation of Heterocycles via C-H Bond Activation: Expanded Scope through Mechanistic Insight.” The Ellman group also developed the chiral amine reagent tert-Butanesulfinamide, which is extensively used in academics and industry for the asymmetric synthesis of amines. A comprehensive survey of tert-Butanesulfinamide methods and applications up through 2009 is provided in the 2010 Chemical Reviews article, “Synthesis and Applications of tert-Butanesulfinamide.”

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