| Weight | 229.324 g/mol |
|---|---|
| Formula | C11H23N3O2 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
1-(2-N-Boc-aminoethyl)piperazine (140447-78-5)
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SMILESCC(C)(C)OC(=O)NCCN1CCNCC1
-
InChIKeyVPOIPCJBJNWHSJ-UHFFFAOYSA-N
Suppliers
Safety
Alternate Names
External Links
Synthesis
Reactant
+
140-31-8
(Schotten-Baumann amide from acyl chloride)
Reactant
+
2-Chloro-2-methylpropane
(Ester from carboxilic acid(SN2))
Similar Compounds
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ethyl 4-methylpiperazine-1-carboxylate
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(120-43-4)
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tert-butyl 4-(bromoacetyl)-1-piperazinecarboxylate
(112257-12-2)
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(7483-27-4)
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(122234-46-2)
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tert-butyl (2-hydrazino-2-oxoethyl)carbamate
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(50606-31-0)
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tert-Butyl (2-(hydroxyamino)-2-iminoethyl)carbamate
(479080-20-1)
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(16066-84-5)
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(75178-87-9)
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(65915-94-8)
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(51644-96-3)
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tert-butyl 3-aminopyrrolidine-1-carboxylate
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tert-Butyl (2-hydrazinyl-2-oxoethyl)(methyl)carbamate
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tert-butyl 3-(piperazin-1-yl)pyrrolidine-1-carboxylate dihydrochloride
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1-Guanyl-4-carbethoxypiperazine sulphate
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(1255717-76-0)
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(301673-14-3)
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(119020-01-8)
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tert-butyl (2S)-2-(aminomethyl)-1-pyrrolidinecarboxylate
(259537-92-3)
1 alternate name
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(S)-(2-Piperidin-3-yl-ethyl)-carbamic acid tert-butyl ester
(215305-98-9)
1 alternate name
3 suppliers
137076-22-3
(137076-22-3)
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3 suppliers
tert-butyl hydroxy(methyl)carbamate
(19689-97-5)
1 alternate name
3 suppliers
1-Boc-3-azetidinone
(398489-26-4)
1 alternate name
3 suppliers
N-Boc-DL-valinol
(169556-48-3)
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tert-butyl (piperidin-3-ylmethyl)carbamate
(142643-29-6)
1 alternate name
3 suppliers
199175-10-5
(199175-10-5)
1 alternate name
3 suppliers
1-(2-N-Boc-aminoethyl)piperazine
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