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CAS No. : | 51857-17-1 | MDL No. : | MFCD00671489 |
Formula : | C11H24N2O2 | Boiling Point : | - |
Linear Structure Formula : | C4H9OC(O)NH(CH2)6NH2 | InChI Key : | RVZPDKXEHIRFPM-UHFFFAOYSA-N |
M.W : | 216.32 | Pubchem ID : | 2733170 |
Synonyms : |
|
Chemical Name : | N-Boc-1,6-Diaminohexane |
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313 | UN#: | N/A |
Hazard Statements: | H315-H319 | Packing Group: | N/A |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
0.9 g | Synthesis of Fmoc-Phe-Gly-NH-(CH2)6NH-Boc To a solution of <strong>[169624-67-3]Fmoc-Phe-Gly-OH</strong> (0.66 g) in anhydrous THF (20 mL) at 0 C. under N2 was added N,N'-dicyclohexylcarbodiimide (0.307 g) and 1-hydroxybenzotriazole hydrate (0.201 g). After stirring for 15 min, N-Boc-1,6-diaminohexane (0.322 g) was added. The reaction mixture was allowed to warm to RT and stirred overnight. Solids were filtered off and they were washed with EtOAc. The filtrate and washings were then concentrated under reduced pressure. The resulting residue was purified by flash column chromatography (0 to 10% MeOH in CH2Cl2) to afford Fmoc-Phe-Gly-NH-(CH2)6NH-Boc as a white solid (0.9 g). |
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