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61985-56-6

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61985-56-6 Usage

Type

Synthetic chemical compound
With psychoactive properties

Mechanism

Potent opioid receptor agonist
Similar in structure to fentanyl (powerful painkiller)

Effects

Euphoria, analgesia, and sedation
Associated with abuse and addiction

Legal status

Schedule I controlled substance in the United States
Illegal to manufacture, distribute, or possess without proper authorization

Medical use

Not approved
Considered to have a high potential for harm

Check Digit Verification of cas no

The CAS Registry Mumber 61985-56-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,8 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61985-56:
(7*6)+(6*1)+(5*9)+(4*8)+(3*5)+(2*5)+(1*6)=156
156 % 10 = 6
So 61985-56-6 is a valid CAS Registry Number.

61985-56-6SDS

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 1-phenyl-2-(piperidin-1-ylmethyl)prop-2-en-1-one,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:61985-56-6 SDS

61985-56-6Relevant articles and documents

N-substituted alpha-aminoalkylacrylophenones and some related compounds: a new class of spermicidal agents.

Gupta,Nautiyal,Jhingran,Kamboj,Setty,Anand

, p. 303 - 307 (2007/10/02)

The results of a screening program to test the spermicidal effectiveness of several compounds is presented. The program was initiated after N-substituted 3-aminoacrylophenones were found to have unexpected spermicidal activity. The compounds had been synthesized as possible antiinflammatory agents. This result prompted the synthesis and screening of N-substituted alpha-aminomethylacrylophenones, alpha-(2-aminomethyl)acrylophenones and 3-N-substituted-2-methyleneindan-1-ones. The starting materials, substituted acetophenones, for the synthesis of N-substituted alpha-aminomethylacrylophenones were either commercial products or obtained by standard methods. N-substituted amino-butyrophenone was reacted with paraformaldehyde to yield the alpha-(2 aminoethyl)acrylophenones. A series of reactions was undertaken to synthesize 2-methyleneindan-1-ones. The preparation of each is detailed and molecular formulas are provided. Spermicidal activity was assessed by dissolving the compound in physiological saline at different concentrations. 2 drops of rat sperm suspension or human semen were placed on a slide, followed by 2 drops of a compound solution. Control slides of physiological saline were prepared. The contents were mixed for approximately 5 seconds and examined under a phase contrast microscope. The results were considered positive if 100% of the spermatozoa became immotile instantaneously. Several of the compounds showed marked spermicidal activity.

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