跳轉至內容
Merck
全部照片(1)

重要文件

查看所有文件

15490

Sigma-Aldrich

Boc-Pro-OH

≥99.0% (T)

同義詞:

N-(叔丁氧羰基)-L-脯氨酸, Boc-L-脯氨酸

登入查看組織和合約定價
全部照片(1)

About This Item

經驗公式（希爾表示法）:
C10H17NO4
CAS號碼:
15761-39-4
分子量：:
215.25
Beilstein:
15828
EC號碼:
239-848-3
MDL號碼:
MFCD00037324
分類程式碼代碼:
12352209
eCl@ss:
32160406
PubChem物質ID:
57647368
NACRES:
NA.22

品質等級

100

化驗

≥99.0% (T)

形狀

solid

光學活性

[α]20/D −61±2°, c = 2% in acetic acid

反應適用性

reaction type: Boc solid-phase peptide synthesis

mp

133-135 °C (lit.)

應用

peptide synthesis

SMILES 字串

CC(C)(C)OC(=O)N1CCC[C@H]1C(O)=O

InChI

1S/C10H17NO4/c1-10(2,3)15-9(14)11-6-4-5-7(11)8(12)13/h7H,4-6H2,1-3H3,(H,12,13)/t7-/m0/s1

InChI 密鑰

ZQEBQGAAWMOMAI-ZETCQYMHSA-N

尋找類似的產品？ 前往 產品比較指南

相關類別

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)

從最近期的版本中選擇一個：

分析證明 (COA)

Lot/Batch Number
BCCH0480
BCCC9557
BCBZ3528
BCBW7782
BCBQ2938V

未看到正確版本？

如果您需要一個特定的版本，您可以透過批號來尋找特定憑證。

搜尋 COA

已經擁有該產品？

您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

Manos Gkikas et al.
Biomacromolecules, 16(11), 3686-3693 (2015-10-16)
Novel poly(L-lysine)-block-poly(L-proline) (PLL-b-PLP)-based materials with all PLP helical conformers, i.e., PLP II and the rare PLP I are here reported. Electrostatic supramolecular complexation of the adjacent cationic PLL with anionic molecules bearing DNA analogue H-bonding functionalities, such as deoxyguanosine monophosphate
Griet Van Zeebroeck et al.
Nature chemical biology, 5(1), 45-52 (2008-12-09)
Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting transceptors is unknown. We have screened 319 amino acid analogs to identify compounds that act on Gap1

文章

Proline Derivatives and Analogs

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.

Natural Amino Acid Building Blocks for Peptide Synthesis

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

Natural Amino Acid Building Blocks for Peptide Synthesis

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

我們的科學家團隊在所有研究領域都有豐富的經驗，包括生命科學、材料科學、化學合成、色譜、分析等.

聯絡技術服務