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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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About This Item

经验公式(希尔记法):
C15H24N2O6
CAS号:
分子量:
328.36
Beilstein:
1505656
MDL號碼:
分類程式碼代碼:
12352209
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

≥98.0% (TLC)

反應適用性

reaction type: Boc solid-phase peptide synthesis

mp

87-92 °C

應用

peptide synthesis

儲存溫度

2-8°C

SMILES 字串

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 密鑰

TYJPSIQEEXOQLC-UHFFFAOYSA-N

其他說明

用于制备荧光探针的交联剂

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Skin Irrit. 2

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

dust mask type N95 (US), Eyeshields, Gloves


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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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