15661
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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关于此项目
经验公式（希尔记法）:
C15H24N2O6
化学文摘社编号:
分子量:
328.36
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1505656
产品名称
Boc-6-Ahx-OSu, ≥98.0% (TLC)
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)
SMILES string
CC(C)(C)OC(=O)NCCCCCC(=O)ON1C(=O)CCC1=O
InChI key
TYJPSIQEEXOQLC-UHFFFAOYSA-N
assay
≥98.0% (TLC)
reaction suitability
reaction type: Boc solid-phase peptide synthesis
mp
87-92 °C
application(s)
peptide synthesis
storage temp.
2-8°C
Quality Level
Other Notes
用于制备荧光探针的交联剂
Hazard Classifications
Skin Irrit. 2
signalword
Warning
hcodes
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
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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