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1-N-Benzyl-3-Hydroxy-Piperidine

1-Benzyl-3-piperidinol

CAS: 14813-01-5

Molecular Formula: C12H17NO

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1-N-Benzyl-3-Hydroxy-Piperidine - Names and Identifiers

Name 1-Benzyl-3-piperidinol
Synonyms 1-Benzyl-3-piperidinol
N-BENZYL-3-PIPERIDINOL
1-BENZYL-3-PIPERIDINOL
N-Benzyl-3-Piperidinol
1-Benzylpiperidin-3-Ol
1-BENZYL-PIPERIDIN-3-OL
1-Benzyl-Piperidin-3-Ol
N-Benzyl-3-Hydroxypiperidine
N-BENZYL-3-HYDROXYPIPERIDINE
1-BENZYL-3-HYDROXYPIPERIDINE
1-Benzyl-3-Hydroxypiperidine
1-Phenylmethyl-3-Piperidinol
3-Piperidinol, 1-Phenylmethyl-
1-N-BENZYL-3-HYDROXY-PIPERIDINE
1-N-Benzyl-3-Hydroxy-Piperidine
Cis-1-Benzyl-2-Methyl-3-Amino Pyrrolidine
CIS-1-BENZYL-2-METHYL-3-AMINO PYRROLIDINE
CAS 14813-01-5
EINECS 238-881-0
InChI InChI=1/C12H17NO/c14-12-7-4-8-13(10-12)9-11-5-2-1-3-6-11/h1-3,5-6,12,14H,4,7-10H2
InChIKey UTTCOAGPVHRUFO-UHFFFAOYSA-N

1-N-Benzyl-3-Hydroxy-Piperidine - Physico-chemical Properties

Molecular FormulaC12H17NO
Molar Mass191.27
Density1,056 g/cm3
Melting Point168-172℃
Boling Point140-142°C 6mm
Flash Point>230°F
Vapor Presure0.000631mmHg at 25°C
AppearancePale yellow to colorless transparent liquid
ColorColorless to Light yellow
BRN135964
pKa14.82±0.20(Predicted)
Storage ConditionInert atmosphere,Room Temperature
SensitiveHygroscopic
Refractive Indexn20/D 1.549

1-N-Benzyl-3-Hydroxy-Piperidine - Risk and Safety

Hazard SymbolsT - Toxic
Toxic
Risk CodesR25 - Toxic if swallowed
R36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
UN IDsUN 2811 6.1/PG 3
WGK Germany2
HS Code29333990

1-N-Benzyl-3-Hydroxy-Piperidine - Reference Information

introduction 1-benzyl -3-piperidinol has a melting point of 168 to 172 degrees, a density of 1.1, and a white solid appearance under normal temperature and pressure. 1-benzyl-3-piperidinol is soluble in common organic solvents, such as dimethyl sulfoxide, N,N-dimethylformamide, dichloromethane, ethyl acetate and alcohols such as methanol and ethanol Solvents, but the solubility in water is poor. It is a common organic synthesis intermediate.
Uses 1-benzyl-3-piperidinol is a common organic synthesis intermediate. First, benzyl can be hydrogenated by palladium and carbon. The group is removed and becomes 3-hydroxypiperidine. Generally speaking, this hydrogenation reaction is simple to operate, and the reaction efficiency is very high, almost no post-treatment is required, so the yield is very high. In addition, the hydroxyl group on the piperidine ring can undergo hydroxyl-related transformations, including conversion to amino groups, oxidation to ketones, and conversion to halogens.
synthesis method dissolve 3-hydroxypiperidine in acetone, add a weak base as an acid binding agent, add the corresponding benzyl bromide, and stir for several hours at room temperature to obtain 1-benzyl-3-piperidinol. It is worth noting that the feeding ratio of the reaction needs to be paid special attention. The amount of benzyl bromide should not be excessive, otherwise it will generate by-products in which the amino and hydroxyl groups are protected by benzyl groups, resulting in a decrease in yield.
environmental hazards 2, 4-dichloro-5-methoxypyrimidine, as an organic compound containing halogen-containing heteroaromatic ring, is more harmful to the water environment. undiluted or a large number of products should not be allowed to contact groundwater, waterways or sewage systems.
Last Update:2024-04-09 20:49:11
1-N-Benzyl-3-Hydroxy-Piperidine
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View History
1-N-Benzyl-3-Hydroxy-Piperidine
Acetic acid, decyl ester
双(环辛酸酯)铁(0)
5-Amino-1-naphthol hydrochloride
beta-D-ribopyranose
Lipoamido-PEG7-azide
4-Amino-3-fluoro phenol
4-溴苯基丙烯酸酯
2,2-Dichloroacetaldehyde
1-AMINOGUANIDINE BICARBONATE
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