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NSC 77933

N-Benzyl-4-piperidone

CAS: 3612-20-2

Molecular Formula: C12H15NO

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NSC 77933 - Names and Identifiers

Name N-Benzyl-4-piperidone
Synonyms NSC 77933
1-Benzylpiperidone
1-Benzyl-4-Pipridine
N-Benzyl-4-Piperidine
N-Benzyl-4-piperidone
1-Benzyl-4-piperidone
N-BENZYL-4-PIPERIDONE
1-Benzylpiperidin-4-one
1-Benzyl-4-piperidinone
1-benzyl-4-oxopiperidine
N- benzylpiperidineketone
1-benzyl-4-oxopiperidinium
1-(Phenylmethyl)-4-piperidinone
1-BENZYL-4-PIPERIDINONE FOR SYNTHESIS
N - benzyl - 4 - piperidine ketone (3612-20-2)
[(4-Oxopiperidin-1-yl)methyl]benzene, 1-Benzyl-4-oxopiperidine
CAS 3612-20-2
EINECS 222-782-4
InChI InChI=1/C12H15NO/c14-12-6-8-13(9-7-12)10-11-4-2-1-3-5-11/h1-5H,6-10H2/p+1

NSC 77933 - Physico-chemical Properties

Molecular FormulaC12H15NO
Molar Mass189.25
Density1.021g/mLat 25°C(lit.)
Boling Point134°C7mm Hg(lit.)
Flash Point>230°F
Water Solubility12 g/L (20 ºC)
Solubility 12g/l
Vapor Presure0.079-0.15Pa at 20-25℃
AppearanceOily Liquid
Specific Gravity1.021
ColorClear colorless to straw
BRN128556
pKa7.07±0.20(Predicted)
Storage Condition2-8°C
Refractive Indexn20/D 1.541(lit.)
Physical and Chemical PropertiesBoiling point 134 ℃(0.93kPa), relative density 1.0523(24/24 ℃), refractive index 1.5399, flash point> 110 ℃.
UseFor the synthesis of the raw material of

NSC 77933 - Risk and Safety

Risk CodesR36/37/38 - Irritating to eyes, respiratory system and skin.
R43 - May cause sensitization by skin contact
R22 - Harmful if swallowed
R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
S37/39 - Wear suitable gloves and eye/face protection
WGK Germany3
HS Code29333999
Hazard NoteIrritant

NSC 77933 - Reference Information

LogP2.1 at 20℃ and pH9
NIST chemical information Information provided by: webbook.nist.gov (external link)
use for the synthesis of penfluridol bulk drug
pharmaceutical intermediates
production method benzylamine is obtained by addition, cyclosynthesis salt, hydrolysis elimination and other steps. 1. N,N-bis (β-methyl propionate) benzylamine was prepared by reaction of addition benzylamine with methyl acrylate. 2. Preparation of 1-benzyl-3-methyl formate piperidone [4] hydrochloride by cyclidiation and salt formation. 3. Hydrolysis and elimination to produce 1-benzylpiperidone [4].
Last Update:2024-04-09 19:05:09
NSC 77933
Supplier List
Shanghai Amole Biotechnology Co., Ltd.
Spot supply
Product Name: 1-Benzylpiperidin-4-one Request for quotation
CAS: 3612-20-2
Tel: 400-968-2212
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Mobile: 18916960931
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MedChemExpress (MCE)
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CAS: 3612-20-2
Tel: 609-228-6898
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     tech@medchemexpress.com
Mobile: 609-228-6898
Shanghai Amole Biotechnology Co., Ltd.
Spot supply
Product Name: 1-Benzylpiperidin-4-one Request for quotation
CAS: 3612-20-2
Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
QQ: 3623107365 Click to send a QQ message
Wechat: 18916960931
MedChemExpress (MCE)
Spot supply
Product Name: 1-Benzyl-4-piperidone Visit Supplier Webpage Request for quotation
CAS: 3612-20-2
Tel: 609-228-6898
Email: sales@medchemexpress.com
     tech@medchemexpress.com
Mobile: 609-228-6898
View History
NSC 77933
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分散黄 55
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