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15661

Sigma-Aldrich

Boc-6-Ahx-OSu

≥98.0% (TLC)

Synonym(s):

6-(Boc-amino)caproic acid N-succinimidyl ester, 6-(Boc-amino)hexanoic acid N-succinimidyl ester

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About This Item

Empirical Formula (Hill Notation):
C15H24N2O6
CAS Number:
51513-80-5
Molecular Weight:
328.36
Beilstein:
1505656
MDL number:
MFCD00237379
UNSPSC Code:
12352209
PubChem Substance ID:
57647512
NACRES:
NA.22

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

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

Other Notes

Linker for preparing fluoroscent probes

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315

Hazard Classifications

Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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