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About This Item
經驗公式（希爾表示法）:
C15H24N2O6
CAS號碼:
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
推薦產品
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
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
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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