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6340-72-3

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6340-72-3 Usage

Chemical Class

Dihydropyrimidines

Medical Use

Anticonvulsant medication

Mode of Action

Stabilizes nerve cell membranes, reduces excessive electrical activity in the brain

Applications

Controls seizures in individuals with epilepsy
Studied for potential use in treating neuropathic pain
Investigated as a neuroprotective agent

Safety Profile

Favorable

Tolerability

Generally well-tolerated

Common Prescription

For management of epilepsy and related conditions

Check Digit Verification of cas no

The CAS Registry Mumber 6340-72-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6340-72:
(6*6)+(5*3)+(4*4)+(3*0)+(2*7)+(1*2)=83
83 % 10 = 3
So 6340-72-3 is a valid CAS Registry Number.

6340-72-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4(1H)-Pyrimidinone, tetrahydro-2-imino-6-phenyl-

1.2 Other means of identification

Product number -
Other names 2-Amino-6-phenyl-5,6-dihydro-3H-pyrimidin-4-on

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:6340-72-3 SDS

6340-72-3Downstream Products

6340-72-3Relevant articles and documents

-

Phillips,Mentha

, p. 574 (1954)

-

Reaction of polyfluorinated chalcones with guanidine

Borodina,Orlova,Gatilov,Sal'Nikova

, p. 1745 - 1752 (2016/02/03)

Reactions of polyfluorinated chalcones with guanidine in the presence of bases are accompanied by elimination of the polyfluorophenyl group. 3-(Pentafluorophenyl)-1-phenylprop-2-en-1-one and its derivatives reacted with guanidine under basic conditions to give 4-phenylpyrimidin-2-amine, polyfluorobenzenes, and Michael adducts, 3-(2-amino-4-phenylpyrimidin-5-yl)-3-(4-R-2,3,5,6-tetrafluorophenyl)-1-phenylpropan-1-ones. 1-(Pentafluorophenyl)-3-phenylprop-2-en-1-one and 1,3-bis(pentafluorophenyl)prop-2-en-1-one were converted into cinnamic acid derivatives whose reaction with guanidine afforded 2-amino-6-aryl-5,6-dihydropyrimidin-4(1H)-ones.

Efficient synthesis of 2-amino-6-aryl-5,6-dihydro -3#-pyrimidin-4-one building blocks via domino reaction

Mohammadnejad, Mahdieh,Hashtroudi, Mehri S.,Balalaie, Saeed

experimental part, p. 459 - 465 (2010/09/20)

One-pot three component condensation of Meldrum's acid, benzaldehyde derivatives and guanidinium carbonate leads to 2-amino-6-aryl-5,6-dihydro-3H- pyrimidin-4-one derivatives in good yields. The products can be utilized in the synthesis of diverse heterocyclic compounds libraries.

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