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47623

Sigma-Aldrich

Fmoc-Tyr(tBu)-OH

≥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

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About This Item

经验公式（希尔记法）:
C28H29NO5
CAS号:
71989-38-3
分子量:
459.53
Beilstein:
4216652
EC號碼:
276-262-7
MDL號碼:
MFCD00037129
分類程式碼代碼:
12352209
eCl@ss:
32160406
PubChem物質ID:
57651043
NACRES:
NA.26

product name

Fmoc-Tyr(tBu)-OH, ≥98.0% (HPLC)

品質等級

100

化驗

≥98.0% (HPLC)

形狀

powder

光學活性

[α]20/D −29±2°, c = 1% in DMF

反應適用性

reaction type: Fmoc solid-phase peptide synthesis

mp

153-156 °C (lit.)

應用

peptide synthesis

官能基

Fmoc

儲存溫度

2-8°C

SMILES 字串

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 密鑰

JAUKCFULLJFBFN-VWLOTQADSA-N

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相关类别

一般說明

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。

應用

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。

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)

从最新的版本中选择一种：

分析证书(COA)

Lot/Batch Number
BCCG9943
BCCC8011
BCCB3701
BCBZ3084
BCBW7539

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