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Merck
CN

440655

Sigma-Aldrich

Boc-Asp(OBzl)-OH

98%

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别名:
N-(叔丁氧羰基)-L-天冬氨酸-4-苄酯, Boc-L-天冬氨酸-4-苄酯
线性分子式:
C6H5CH2OCOCH2CH(COOH)NHCOOC(CH3)3
CAS号:
分子量:
323.34
Beilstein:
2064127
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:

检测方案

98%

旋光性

[α]20/D −19.5°, c = 2 in DMF

mp

98-102 °C (lit.)

SMILES字符串

[H][C@@](CC(=O)OCc1ccccc1)(NC(=O)OC(C)(C)C)C(O)=O

InChI

1S/C16H21NO6/c1-16(2,3)23-15(21)17-12(14(19)20)9-13(18)22-10-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,21)(H,19,20)/t12-/m0/s1

InChI key

SOHLZANWVLCPHK-LBPRGKRZSA-N

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应用

用于光学异构合成 (R)-(+)-Boc-iturinic acid (n-C14)、L-天冬氨酸系列凝血酶抑制剂,以及二酮哌嗪四肽的原料。用于制备位于 [6H]-氮杂卓并吲哚啉中心的新型模拟三环二肽。

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

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Bergeron, R.J. et al.
Journal of the American Chemical Society, 116, 8479-8479 (1994)
K Hilpert et al.
Journal of medicinal chemistry, 37(23), 3889-3901 (1994-11-11)
Thrombin, a serine protease, plays a central role in the initiation and propagation of thrombotic events. An extensive search for new thrombin inhibitors was performed, using an unconventional approach. Screening of small basic molecules for binding in the recognition pocket
De Lombaert, S. et al.
Tetrahedron Letters, 35, 7513-7513 (1994)
Nicole Niklas et al.
Dalton transactions (Cambridge, England : 2003), (1)(1), 154-162 (2006-12-13)
The amino acid derivative Boc-Asp-OBzl (Boc=N-butyloxycarbonyl; Asp=aspartic acid; Bzl=benzyl) was functionalized by coupling its carboxylate side chain to dipicolylamine. This yielded the tridentate nitrogen donor ligand Boc-Asp(Dpa)-OBzl (-OBzl). The compound -OBzl contains three different carbonyl groups: a tertiary amide linkage
Vitamin K1 dependent carboxylase: beta-carboxylation of t-butyloxycarbonylaspartic acid alpha-benzyl ester.
S E Hamilton et al.
Biochemical and biophysical research communications, 107(1), 246-249 (1982-07-16)

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