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67051-21-2

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67051-21-2 Usage

Class of Medication

Hydantoin anticonvulsant

Therapeutic Use

Treatment of epilepsy and seizures

Mechanism of Action

Stabilizes electrical activity in the brain, preventing seizures

Forms Available

Tablets, capsules, suspension

Administration Route

Oral (taken by mouth)

Therapeutic Index

Relatively narrow, necessitating blood level monitoring

Adverse Effects

Dizziness, drowsiness, nausea, among others

Importance

Significant medication for managing specific types of seizures and epilepsy

Check Digit Verification of cas no

The CAS Registry Mumber 67051-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,5 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67051-21:
(7*6)+(6*7)+(5*0)+(4*5)+(3*1)+(2*2)+(1*1)=112
112 % 10 = 2
So 67051-21-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H20N2O3/c1-2-3-4-8-11-16(12-9-6-5-7-10-12)13(19)17-15(21)18-14(16)20/h5-7,9-10H,2-4,8,11H2,1H3,(H2,17,18,19,20,21)

67051-21-2SDS

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 5-hexyl-5-phenyl-1,3-diazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names BARBITURIC ACID,5-HEXYL-5-PHENYL

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:67051-21-2 SDS

67051-21-2Downstream Products

67051-21-2Relevant articles and documents

Novel 5,5-disubstitutedpyrimidine-2,4,6-triones as selective MMP inhibitors

Foley, Louise H,Palermo, Robert,Dunten, Pete,Wang, Ping

, p. 969 - 972 (2007/10/03)

The 5,5-disubstitutedpyrimidine-2,4,6-triones represent a new class of MMP inhibitors showing selectivity for the gelatinases A and B, collagenase-3, and human neutrophil collagenase. The SAR presented here is in good agreement with an X-ray structure of compound 5 bound to the catalytic domain of stromelysin-1. While of the barbiturate structural class, compound 5 did not show any toxic or sedative effects.

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