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3-Nitrophencyclidine is a chemical compound with the molecular formula C7H10N2O3. It is a derivative of phencyclidine (PCP), a dissociative anesthetic with hallucinogenic properties. The compound features a nitro group (-NO2) attached to the 3-position of the phencyclidine molecule, which significantly alters its pharmacological profile compared to its parent compound. 3-Nitrophencyclidine is known for its potent psychoactive effects, and it is classified as a controlled substance due to its potential for abuse and harmful health effects. It is important to note that the use, possession, and distribution of 3-Nitrophencyclidine are illegal in many countries, and it should not be used for recreational or medicinal purposes without proper medical supervision.

70227-29-1

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70227-29-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70227-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,2,2 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70227-29:
(7*7)+(6*0)+(5*2)+(4*2)+(3*7)+(2*2)+(1*9)=101
101 % 10 = 1
So 70227-29-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H24N2O2/c20-19(21)16-9-7-8-15(14-16)17(10-3-1-4-11-17)18-12-5-2-6-13-18/h7-9,14H,1-6,10-13H2

70227-29-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-nitrophencyclidine

1.2 Other means of identification

Product number -
Other names 1-[1-(3-nitro-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:70227-29-1 SDS

70227-29-1Upstream product

70227-29-1Relevant academic research and scientific papers

Syntheses of Amine Derivatives of Phencyclidine

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

, p. 2049 - 2054 (2007/10/02)

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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