14972
Boc-8-Aoc-OH
≥97.0%
Synonym(s):
8-(Boc-amino)caprylic acid, 8-(Boc-amino)octanoic acid
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About This Item
Linear Formula:
(CH3)3CO2CNH(CH2)7CO2H
CAS Number:
Molecular Weight:
259.34
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2268966
InChI
1S/C13H25NO4/c1-13(2,3)18-12(17)14-10-8-6-4-5-7-9-11(15)16/h4-10H2,1-3H3,(H,14,17)(H,15,16)
SMILES string
CC(C)(C)OC(=O)NCCCCCCCC(O)=O
InChI key
FPRZYWCRQHFPSX-UHFFFAOYSA-N
assay
≥97.0%
reaction suitability
reaction type: Boc solid-phase peptide synthesis
mp
56-59 °C
application(s)
peptide synthesis
Other Notes
Reagent to introduce a protected ω-amino alkyl spacer. Longer spacer arms often impart increased activity to the substrate.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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B J Bradbury et al.
Journal of medicinal chemistry, 33(2), 741-748 (1990-02-01)
A functionalized congener approach was used to design ligands for muscarinic cholinergic receptors (mAChRs). A series of omega-functionalized alkyl amides of N-methyl-4-(1-pyrrolidinyl)-2-butynamine (22) were prepared as functionalized analogues of UH 5 [N-methyl-N-[4-(1-pyrrolidinyl)-2-butynyl]acetamide], a muscarinic agonist related to oxotremorine. Intermediate 22
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