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3-Phenyl-propionamidine HCl, also known as phenprobamate hydrochloride, is a synthetic chemical compound belonging to the class of organic compounds known as aryl-phenylketones. It functions as a central nervous system depressant and muscle relaxant, and is utilized as a sedative and anxiolytic medication.
Used in Pharmaceutical Industry:
3-Phenyl-propionamidine HCl is used as a sedative and anxiolytic for the treatment of anxiety, tension, and muscle spasms due to its ability to influence neurotransmitters in the brain and enhance the inhibitory effects of gamma-aminobutyric acid (GABA).
Used in Neurological Treatments:
3-Phenyl-propionamidine HCl is used as a muscle relaxant to alleviate muscle spasms, potentially due to its effects on the central nervous system and its interaction with neurotransmitters.
Used in Anticonvulsant Therapy:
3-Phenyl-propionamidine HCl is used as an anticonvulsant, likely due to its sedative properties and its ability to stabilize neuronal activity, thus preventing seizures.

24441-89-2

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24441-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24441-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,4 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24441-89:
(7*2)+(6*4)+(5*4)+(4*4)+(3*1)+(2*8)+(1*9)=102
102 % 10 = 2
So 24441-89-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H3,10,11)

24441-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylpropanimidamide,hydrochloride

1.2 Other means of identification

Product number -
Other names 3-Phenyl-propionamidin,Hydrochlorid

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:24441-89-2 SDS

24441-89-2Relevant academic research and scientific papers

The Preparation and Liquid Crystal Behaviour of Pyrimidines and Dioxans Incorporating a Dimethylene Linking Group

Andrews, B. M.,Gray, G. W.,Bradshaw, M. J.

, p. 257 - 270 (2007/10/02)

The preparation of 2-(4-cyanophenylethyl)-5-alkylpyrimidines and trans-2-(4-(cyanophenylethyl)-5-alkyl-1,3-dioxans, which incorporate a dimethylene linking group into phenylpyrimidine and phenyldioxan structures, is described.The pyrimidinyl compounds exhibit only virtual nematic-isotropic transitions and the dioxan compounds have monotropic nematic-isotropic transitions.Comparisons are made between the liquid crystal behaviour of these compounds and similar materials not incorporating the linking group.Comparisons are also made with related systems incorporating the bicyclo(2.2.2) octane ring and with systems in which the dimethylene group links two phenyl rings.The materials described have been found to exhibit interesting dielectric properties.The pyrimidine compounds, for example, have higher perpendicular and parallel permittivities than corresponding materials without the dimethylene linkage.

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