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Merck

531480

Sigma-Aldrich

N-芴甲氧羰基-L-丙氨酸

95%, for peptide synthesis

别名:

N-芴甲氧羰基-L-丙氨酸, Fmoc-L-丙氨酸

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About This Item

经验公式(希尔记法):
C18H17NO4
CAS号:
分子量:
311.33
Beilstein:
2225975
EC號碼:
MDL號碼:
分類程式碼代碼:
12352209
PubChem物質ID:
NACRES:
NA.26

产品名称

N-芴甲氧羰基-L-丙氨酸, 95%

化驗

95%

光學活性

[α]20/D −18°, c = 1 in DMF

反應適用性

reaction type: C-H Activation
reaction type: Fmoc solid-phase peptide synthesis
reagent type: ligand
reaction type: Peptide Synthesis

mp

147-153 °C (lit.)

應用

peptide synthesis

官能基

Fmoc
amine
carboxylic acid

儲存溫度

2-8°C

SMILES 字串

C[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C18H17NO4/c1-11(17(20)21)19-18(22)23-10-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,11,16H,10H2,1H3,(H,19,22)(H,20,21)/t11-/m0/s1

InChI 密鑰

QWXZOFZKSQXPDC-NSHDSACASA-N

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一般說明

Fmoc-Ala-OH又称为Fmoc-L-丙氨酸, 在Fmoc固相肽合成中起多种作用。

應用

Fmoc-Ala-OH的一般用途:
  • 作为制备三唑肽和氮杂肽的构件
  • 通过标准Fmoc固相肽合成法合成双阳离子卟啉肽
  • 不经过氮杂环丙烷化作用,将曼尼希加合物转化为α-卤化酰胺

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)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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商品

With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.

With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.

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