主要文件

查看所有文档

47623

Fmoc-Tyr(tBu)-OH

Name: Fmoc-Tyr(<I>t</I>Bu)-OH
Brand: ALDRICH

≥98.0% (HPLC), for peptide synthesis

别名:

N-(9-芴甲氧羰基)-O-叔丁基-L-酪氨酸, Fmoc-O-叔丁基-L-酪氨酸

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

经验公式（希尔记法）:

C₂₈H₂₉NO₅

化学文摘社编号:

71989-38-3

分子量:

459.53

NACRES:

NA.26

PubChem Substance ID:

57651043

eCl@ss:

32160406

UNSPSC Code:

12352209

EC Number:

276-262-7

MDL number:

MFCD00037129

Beilstein/REAXYS Number:

4216652

技术服务

需要帮助？我们经验丰富的科学家团队随时乐意为您服务。

让我们为您提供帮助

属性

产品名称

Fmoc-Tyr(tBu)-OH, ≥98.0% (HPLC)

Quality Level

100

assay

≥98.0% (HPLC)

form

powder

optical activity

[α]20/D −29±2°, c = 1% in DMF

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

mp

153-156 °C (lit.)

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

CC(C)(C)Oc1ccc(C[C@H](NC(=O)OCC2c3ccccc3-c4ccccc24)C(O)=O)cc1

InChI

1S/C28H29NO5/c1-28(2,3)34-19-14-12-18(13-15-19)16-25(26(30)31)29-27(32)33-17-24-22-10-6-4-8-20(22)21-9-5-7-11-23(21)24/h4-15,24-25H,16-17H2,1-3H3,(H,29,32)(H,30,31)/t25-/m0/s1

InChI key

JAUKCFULLJFBFN-VWLOTQADSA-N

说明

General description

Fmoc-Tyr(tBu)-OH也称为Fmoc-O-叔丁基-L-酪氨酸，通常用于Fmoc固相法肽合成。

Application

Fmoc-Tyr(tBu)-OH可用于通过水中固相反应合成亮氨酸-脑啡肽酰胺(Leu-Enkephalin Amide)。也用于合成氨基酸衍生物，例如Fmoc-Tyr-OAllyl。

Still not finding the right product?

Explore all of our products under Fmoc-Tyr(tBu)-OH

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

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。

搜索COA

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

Absolute Quantitation of Glycoforms of Two Human IgG Subclasses Using Synthetic Fc Peptides and Glycopeptides.

Rini Roy et al.

Journal of the American Society for Mass Spectrometry, 29(6), 1086-1098 (2018-05-26)

Immunoglobulins, such as immunoglobulin G (IgG), are of prime importance in the immune system. Polyclonal human IgG comprises four subclasses, of which IgG1 and IgG2 are the most abundant in healthy individuals. In an effort to develop an absolute MALDI-ToF-MS

Protected Amino Acid-Based Hydrogels Incorporating Carbon Nanomaterials for Near-Infrared Irradiation-Triggered Drug Release.

Chloé Guilbaud-Chéreau et al.

ACS applied materials & interfaces, 11(14), 13147-13157 (2019-03-14)

Molecular gels formed by the self-assembly of low-molecular-weight gelators have received increasing interest because of their potential applications in drug delivery. In particular, the ability of peptides and amino acids to spontaneously self-assemble into three-dimensional fibrous network has been exploited

A New Caged-Glutamine Derivative as a Tool To Control the Assembly of Glutamine-Containing Amyloidogenic Peptides.

Loay Awad et al.

Chembiochem : a European journal of chemical biology, 17(24), 2353-2360 (2016-10-28)

We present the design, synthesis, and characterization of a novel photocaged glutamine derivative (modified on the side chain of glutamine), and describe its use in enhancing peptide stability and solubility. Our results demonstrate that this approach can be used to

查看所有相关文献

全球贸易项目编号

货号	GTIN
47623-10G-F	04061832362199
47623-1KG-F	04061826222683
47623-100G-F	04061832362182
47623-25G-F	04061832362205