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2201-33-4

Piperidine, 1-[1-(4-bromophenyl)cyclohexyl]-, is a complex organic compound with the chemical formula C18H24BrN. It is a derivative of piperidine, a heterocyclic amine, and features a cyclohexyl group substituted with a 4-bromophenyl moiety. Piperidine,1-[1-(4-bromophenyl)cyclohexyl]- is characterized by its unique molecular structure, which consists of a six-membered nitrogen-containing ring (piperidine) and a six-membered carbon ring (cyclohexane) connected through a single carbon-carbon bond. The presence of the bromine atom in the 4-position of the phenyl group adds a halogenated feature to the molecule, which can influence its reactivity and physical properties. Piperidine,1-[1-(4-bromophenyl)cyclohexyl]- may be used in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its structural diversity and potential for further functionalization.

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  • 2201-33-4 Structure

  • Basic information

    1. Product Name: Piperidine,1-[1-(4-bromophenyl)cyclohexyl]-
    2. Synonyms: Piperidine,1-[1-(p-bromophenyl)cyclohexyl]- (7CI,8CI); WL 32669
    3. CAS NO:2201-33-4
    4. Molecular Formula: C17H24 Br N
    5. Molecular Weight: 322.288
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2201-33-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Piperidine,1-[1-(4-bromophenyl)cyclohexyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Piperidine,1-[1-(4-bromophenyl)cyclohexyl]-(2201-33-4)
    11. EPA Substance Registry System: Piperidine,1-[1-(4-bromophenyl)cyclohexyl]-(2201-33-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2201-33-4(Hazardous Substances Data)

2201-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2201-33-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2201-33:
(6*2)+(5*2)+(4*0)+(3*1)+(2*3)+(1*3)=34
34 % 10 = 4
So 2201-33-4 is a valid CAS Registry Number.

2201-33-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromophencyclidine

1.2 Other means of identification

Product number -
Other names 1-[1-(4-bromo-phenyl)-cyclohexyl]-piperidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2201-33-4 SDS

2201-33-4Relevant articles and documents

Syntheses of Amine Derivatives of Phencyclidine

Johnson, Peter Y.,Pan, Robert,Wen, Jing Quan,Halfman, Clarke J.

, p. 2049 - 2054 (1981)

3-Aminophencyclidine (5) was synthesized by reduction of 3-nitrophencyclidine (3) using either H2 with Pd/C or Na2S in refluxing methanol.Attempts to isolate 4-aminophencyclidine (2), which we hoped to synthesize by hydrolysis of carbamate 15 which was isolated after reaction of amide 10 under Hofmann conditions employing bromine in CH3O(1-)/CH3OH at -40 deg C, were unsuccessful. 4-Aminomethylphencyclidine (18) was synthesized by LAH reduction of nitrile 13 as well as by reductive amination of aldehyde 20.Nitrile 13 and aldehyde 20 were synthesized from 4-bromophencyclidine (11) as was alcohol 26 which served as a precursor to 4-(2-aminoethyl)phencyclidine (19).Amine 19 was also synthesized by NaBH4 reduction of β-nitrostyrene 29 which was generated from aldehyde 20 by condensation with nitromethane using 1,5-diazabicycloundecene as the base catalyst followed by LAH reduction of resulting 4-(2-nitroethyl)phencyclidine (30).Mass spectra and 13C NMR spectra have been obtained on most of the phencyclidine derivatives.

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