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Methiotriazamine hydrochloride is a chemical compound with the molecular formula C4H10ClN3S. It is a derivative of methiotriazamine, an organic compound that belongs to the class of triazoles. Methiotriazamine hydrochloride is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of fungicides. It is known for its ability to inhibit the biosynthesis of ergosterol, an essential component of fungal cell membranes, thereby exhibiting antifungal properties. The hydrochloride salt form of methiotriazamine enhances its solubility and stability, making it more suitable for industrial applications.

6043-86-3

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6043-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6043-86-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,4 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6043-86:
(6*6)+(5*0)+(4*4)+(3*3)+(2*8)+(1*6)=83
83 % 10 = 3
So 6043-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H17N5S/c1-12(2)16-10(13)15-11(14)17(12)8-4-6-9(18-3)7-5-8/h4-7H,1-3H3,(H4,13,14,15,16)

6043-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,6-dimethyl-1-(4-methylsulfanylphenyl)-1,3,5-triazine-2,4-diamine,hydrochloride

1.2 Other means of identification

Product number -
Other names Methiotriazamine hydrochloride

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:6043-86-3 SDS

6043-86-3Downstream Products

6043-86-3Relevant academic research and scientific papers

Quantitative Structure-Activity Relationships of the Inhibition of Pneumocystis carinii Dihydrofolate Reductase by 4,6-Diamino-1,2-dihydro-2,2-dimethyl-1-(X-phenyl)-s-triazines

Marlowe, Charles K.,Selassie, Cynthia Dias,Santi, Daniel V.

, p. 967 - 972 (2007/10/02)

The inhibitory activities of 60 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-(X-phenyl)-s-triazines versus purified, recombinant Pneumocystis carinii (Pc) dihydrofolate reductase (DHFR) have been determined at pH 7.0.Utilization of these Kiapp values has led to the formulation of appropriate quantitative structure-activity relationships (QSAR's) for both meta- and para-substituted derivatives.The QSAR's from Pc are compared with other triazine QSAR's derived versus chicken, murine tumor, Escherichia coli, and particularly human DHFR.Selectivity indices indicate that hydrophobic triazines are particularly effective versus Pc DHFR; they have lower Ki values for Pc DHFR than for human DHFR.

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