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Merck

15661

Sigma-Aldrich

Boc-6-Ahx-OSu

≥98.0% (TLC)

别名:

6-(Boc-氨基)己酸N-琥珀酰亚胺酯, 6-(Boc-氨基)羊油酸N-琥珀酰亚胺酯

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5 G
$496.00

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5 G
$496.00

About This Item

经验公式(希尔记法):
C15H24N2O6
CAS号:
分子量:
328.36
Beilstein:
1505656
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.22

$496.00


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方案

≥98.0% (TLC)

反应适用性

reaction type: Boc solid-phase peptide synthesis

mp

87-92 °C

应用

peptide synthesis

储存温度

2-8°C

SMILES字符串

CC(C)(C)OC(=O)NCCCCCC(=O)ON1C(=O)CCC1=O

InChI

1S/C15H24N2O6/c1-15(2,3)22-14(21)16-10-6-4-5-7-13(20)23-17-11(18)8-9-12(17)19/h4-10H2,1-3H3,(H,16,21)

InChI key

TYJPSIQEEXOQLC-UHFFFAOYSA-N

其他说明

用于制备荧光探针的交联剂[1][2]

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Skin Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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M A Juliano et al.
The journal of peptide research : official journal of the American Peptide Society, 53(2), 109-119 (1999-04-09)
We synthesized short chromogenic peptidyl-Arg-p-nitroanilides containing either (Galbeta)Ser or (Glcalpha,beta)Tyr at P2 or P3 sites as well as O-acetylated sugar moieties and studied their hydrolysis by bovine trypsin, papain, human tissue kallikrein and rat tonin. For comparison, the susceptibility to
M Adamczyk et al.
Steroids, 62(6), 462-467 (1997-06-01)
6-Oxoestradiol (2) was protected as its bis[(2-trimethylsilylethoxy)methyl] ether (4) and converted to the corresponding oxime (4). The oxime (4) on reduction with zinc in ethanol afforded the bis-SEM ether of 6-alpha-aminoestradiol (5) in 96% epimeric excess. Subsequently, 5 was hydrolyzed

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