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N,N-???????-4-??

N,N-???????-4-??
N,N-???????-4-?? ??? ???
?? ??:
50533-97-6
???:
N,N-???????-4-??
???(??):
N,N-???????-4-??
???:
N,N-Dimethylpiperidin-4-amine
???(??):
DIMETHYL-PIPERIDIN-4-YL-AMINE;EOS-60858;AKOS BB-9178;CHEMBRDG-BB 4018153;4-DIMETHYLAMINO-PIPERIDINE;N,N-Dimethylpiperidin-4-amin;N,N-DIMETHYLPIPERIDIN-4-AMINE;N,N-Dimethyl-4-piperidinamine;N,N''-DIMETHYLAMINOPIPERIDINE;4-DIMETHYLAMINO-PIPERIDINE 98%
CBNumber:
CB0394628
???:
C7H16N2
??? ??:
128.22
MOL ??:
50533-97-6.mol
MSDS ??:
SDS

N,N-???????-4-?? ??

?? ?
187°C
??
1.09g/ml
???
187°C
???
1.4760
?? ??
under inert gas (nitrogen or Argon) at 2–8 °C
??? ??
??
?? ?? (pKa)
10.10±0.10(Predicted)
??
Clear, colourless
BRN
1190
InChI
InChI=1S/C7H16N2/c1-9(2)7-3-5-8-6-4-7/h7-8H,3-6H2,1-2H3
InChIKey
YFJAIURZMRJPDB-UHFFFAOYSA-N
SMILES
N1CCC(N(C)C)CC1
CAS ??????
50533-97-6(CAS DataBase Reference)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? Xi,Xn
?? ???? ?? 10-34-22
????? 26-36/37/39-45
????(UN No.) 2734
?? ?? ?? Irritant
?? ?? 8
???? III
HS ?? 2933399990
????(GHS): GHS hazard pictograms
?? ?: Danger
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H314 ??? ?? ??? ?? ??? ??? ????? ?? ????? ?? 1A, B, C ?? GHS hazard pictograms P260,P264, P280, P301+P330+ P331,P303+P361+P353, P363, P304+P340,P310, P321, P305+ P351+P338, P405,P501
H318 ?? ?? ??? ??? ?? ? ?? ?? ??? ?? ?? 1 ?? GHS hazard pictograms P280, P305+P351+P338, P310
??????:
P301+P330+P331 ???? ?? ?????. ??? ?? ?? ???.
P303+P361+P353 ??(?? ????)? ??? ??? ?? ??? ??? ????? ??? ?? ????/?????.
P305+P351+P338 ?? ??? ? ?? ?? ???? ????. ???? ?????? ?????. ?? ????.
P405 ???? ?????.
NFPA 704
0
1 0

N,N-???????-4-?? C??? ??, ??, ??

??

4-(Dimethylamino)piperidine is having molecular features associated with polyamine modulation of N-methyl-D-aspartate receptors. It is utilized as a mechanism for reducing the effects of alcohol dependence.

Synthesis

2.jpg
1-(tert-Butoxycarbonyl)-4-piperidone (998 mg, 4.75 mmol) in methanol (15 mL) was treated with dimethylamine hydrochloride (800 mg, 9.8 mmol) and sodium cyanoborohydride (270 mg, 4.3 mmol) at rt. After 4 days, concentrated HCl (10 mL) was added and the reaction was reduced in vacuo. The resulting residue was dissolved in H2O (30 mL) and treated with 2M NaOH solution to achieve a pH of 10. The aqueous solution was extracted with methylene chloride (3×20 mL) and the combined organics were dried over Na2SO4 and removed in vacuo. The resulting product is N,N-Dimethylpiperidin-4-amine (169 mg).

N,N-???????-4-?? ?? ?? ? ???

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N,N-???????-4-?? ?? ??

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