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Merck
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47636

Sigma-Aldrich

芴甲氧羰基-L-脯氨酸

≥90% (HPLC)

同義詞:

N-(9-芴甲氧羰基)-L-脯氨酸, Fmoc-L-脯氨酸

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About This Item

經驗公式(希爾表示法):
C20H19NO4
CAS號碼:
分子量::
337.37
Beilstein:
3596735
EC號碼:
MDL號碼:
分類程式碼代碼:
12352209
eCl@ss:
32160406
PubChem物質ID:
NACRES:
NA.26

化驗

≥90% (HPLC)

光學活性

[α]20/D −32±1°, c = 1% in DMF

反應適用性

reaction type: Fmoc solid-phase peptide synthesis

mp

117-118 °C (lit.)

應用

peptide synthesis

官能基

Fmoc

儲存溫度

2-8°C

SMILES 字串

OC(=O)[C@@H]1CCCN1C(=O)OCC2c3ccccc3-c4ccccc24

InChI

1S/C20H19NO4/c22-19(23)18-10-5-11-21(18)20(24)25-12-17-15-8-3-1-6-13(15)14-7-2-4-9-16(14)17/h1-4,6-9,17-18H,5,10-12H2,(H,22,23)/t18-/m0/s1

InChI 密鑰

ZPGDWQNBZYOZTI-SFHVURJKSA-N

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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)


分析證明 (COA)

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文章

Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.

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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