15661
Boc-6-Ahx-OSu
≥98.0% (TLC)
동의어(들):
6-(Boc-amino)caproic acid N-succinimidyl ester, 6-(Boc-amino)hexanoic acid N-succinimidyl ester
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C15H24N2O6
CAS Number:
Molecular Weight:
328.36
Beilstein:
1505656
MDL number:
UNSPSC 코드:
12352209
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
≥98.0% (TLC)
반응 적합성
reaction type: Boc solid-phase peptide synthesis
mp
87-92 °C
응용 분야
peptide synthesis
저장 온도
2-8°C
SMILES string
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
기타 정보
Linker for preparing fluoroscent probes
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
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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