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位置: 首页> 品牌> Sigma-Aldrich> Nα-(9-芴甲氧羰基)-Nγ-三苯甲基- L -天冬酰胺

Fmoc-Asn(Trt)-OH

Nα-(9-Fluorenylmethoxycarbonyl)-Nγ-trityl- L -asparagine

品牌
Sigma-Aldrich
CAS
132388-59-1
货号
47672
规格纯度
≥97.0%
价格
637.74 *本价格含增值税费
促销
服务
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  • 增值税票
数量
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半岛bd体育手机客户端 名称:
132388-59-1
Fmoc-Asn(Trt)-OH
Nα-(9-Fluorenylmethoxycarbonyl)- Nγ-trityl- L -asparagine
Nα-Fmoc- Nγ-trityl- L -asparagine
Nα-(9-芴甲氧羰基)- Nγ-三苯甲基- L -天冬酰胺
Nα-Fmoc- Nγ-三苯甲基- L -天冬酰胺
半岛bd体育手机客户端 介绍:

半岛bd体育手机客户端 说明

一般描述

Fmoc-Asn(Trt)-OH has good solubility properties in most organic solvents, and its use has been shown to result in significantly purer peptides than other derivatives used for the introduction of Asn [1, 2]. Coupling can be performed by standard procedures. The trityl group is normally removed by 95% TFA in 1-3 hours, with no alkylation of Trp residues. When Asn(Trt) is the N-terminal residue, the reaction time may need to be extended to ensure complete deprotection [3].

应用

Fmoc-Asn(Trt)-OH has been used to synthesize peptides on cellulose membrane by SPOT method

包装

5, 25, 100 g in poly bottle
1 kg in poly bottle

基本信息

经验(实验)分子式 C38H32N2O5
分子量 596.67
Beilstein 4343823
MDL编号 MFCD00077049
eCl@ss 32160406
PubChem化学物质编号 57651076
NACRES NA.26

半岛bd体育手机客户端 性质

质量水平 100
测定 ≥97.0%
旋光性 [α]20/D ?15.0±1°, c = 1% in methanol
reaction suitability reaction type: Fmoc solid-phase peptide synthesis
mp 201-204 ℃ (lit.)
application(s) peptide synthesis
官能团 Fmoc
储存温度 2-8℃
SMILES string OC(=O)[C@H](CC(=O)NC(c1ccccc1)(c2ccccc2)c3ccccc3)NC(=O)OCC4c5ccccc5-c6ccccc46
InChI 1S/C38H32N2O5/c41-35(40-38(26-14-4-1-5-15-26,27-16-6-2-7-17-27)28-18-8-3-9-19-28)24-34(36(42)43)39-37(44)45-25-33-31-22-12-10-20-29(31)30-21-11-13-23-32(30)33/h1-23,33-34H,24-25H2,(H,39,44)(H,40,41)(H,42,43)/t34-/m0/s1
InChI key KJYAFJQCGPUXJY-UMSFTDKQSA-N

安全信息

象形图 GHS09
危险声明 H411
危险分类 Aquatic Chronic 2
储存分类代码 13 - Non Combustible Solids
WGK WGK 2
闪点(F) Not applicable
闪点(C) Not applicable
个人防护装备 Eyeshields, Gloves, type N95 (US)

Sigma-Aldrich

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