ChemicalBook--->CAS DataBase List--->169448-87-7

169448-87-7

169448-87-7 Structure

169448-87-7 Structure
IdentificationBack Directory
[Name]

(R)-1-N-Boc-2-(hydroxymethyl)piperazine
[CAS]

169448-87-7
[Synonyms]

Nicotinamide Impurity 202
(R)-1-Boc-2-(hyroxyMethyl)piperazine
(R)-1-Boc-2-Hydroxymethyl-piperazine
(R)-1-N-BOC-2-HYDROXYMETHYLPIPERAZINE HCl
(R)-1-Boc-2-Hydroxymethyl-piperazine ,98%
(S)-1-Boc-2-Hydroxymethyl-piperazine ,98%
tert-butyl (R)-2-(hydroxymethyl)piperazine-1-carboxylate
(R)-tert-Butyl 2-(hydroxymethyl)piperazine-1-carboxylate
tert-Butyl (2R)-2-(hydroxymethyl)piperazin-1-carboxylate
tert-Butyl (2R)-2-(hydroxymethyl)piperazine-1-carboxylate
2-Methyl-2-propanyl(2R)-2-(hydroxymethyl)-1-piperazinecarboxylate
(2R)-2-(hydroxymethyl)-1-Piperazinecarboxylic acid tert-butyl ester
1-Piperazinecarboxylic acid, 2-(hydroxymethyl)-, 1,1-dimethylethyl ester, (2R)-
(R)-1-N-Boc-2-(hydroxymethyl)piperazine###(R)-2-HYDROXYMETHYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
[Molecular Formula]

C10H20N2O3
[MDL Number]

MFCD07772092
[MOL File]

169448-87-7.mol
[Molecular Weight]

216.28
Chemical PropertiesBack Directory
[Boiling point ]

324.0±17.0 °C(Predicted)
[density ]

1.085±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,2-8°C
[pka]

14.97±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HS Code ]

2933599590
Hazard InformationBack Directory
[Uses]

(R)-tert-Butyl 2-(hydroxymethyl)piperazine-1-carboxylate is used in preparation of novel substituted quinoline-8-carbonitrile derivatives with androgen receptor degradation activity and uses thereof.
[Synthesis]

Lithium aluminum hydride (1M in THF, 26 ml) was added to a solution of L-TERT- butyl 2-methyl (2R)-piperazine-1, 2-dicarboxylate (2. 55 g) in THF (70 ml) at-40°C, and then the reaction was warmed to room temperature. After stirring for 1 h, this reaction system was cooled to 0°C and quenched by sequential addition of water (1 ml), sodium hydroxide (2N, 1 ml), and then water (2 ml). The resulting slurry was filtered and concentrated in vacuo to give (R)-1-N-Boc-2-(hydroxymethyl)piperazine.
(R)-1-N-Boc-2-(hydroxymethyl)piperazine
Spectrum DetailBack Directory
[Spectrum Detail]

(R)-1-N-Boc-2-(hydroxymethyl)piperazine(169448-87-7)1HNMR
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