95037-20-0 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
(3-aMino-5,6-dichloropyrazin-2-yl)Methanol is used as a key intermediate in the synthesis of various pharmaceutical compounds for its unique structural and functional characteristics. Its amino and hydroxyl groups can be exploited in the design and development of new drugs, potentially leading to innovative therapeutic agents with improved efficacy and selectivity.
Used in Organic Synthesis:
In the field of organic synthesis, (3-aMino-5,6-dichloropyrazin-2-yl)Methanol serves as a versatile building block for the creation of a wide range of organic compounds. Its reactive functional groups allow for various chemical reactions, such as nucleophilic substitution, acylation, and alkylation, enabling the synthesis of complex organic molecules with diverse applications.
Used in Chemical Research:
(3-aMino-5,6-dichloropyrazin-2-yl)Methanol is utilized as a research tool in chemical studies, providing insights into the reactivity and properties of pyrazine derivatives. Its unique structure allows researchers to explore novel reaction pathways and mechanisms, contributing to the advancement of chemical knowledge and the discovery of new synthetic methods.
Used in Material Science:
In material science, (3-aMino-5,6-dichloropyrazin-2-yl)Methanol may find applications in the development of new materials with specific properties, such as high thermal stability, chemical resistance, or unique electronic characteristics. Its functional groups can be incorporated into polymers, coatings, or other materials to impart desired attributes or improve performance.
Used in Environmental Applications:
(3-aMino-5,6-dichloropyrazin-2-yl)Methanol could potentially be employed in environmental applications, such as the remediation of contaminated sites or the development of eco-friendly materials. Its chemical properties may enable it to interact with pollutants or hazardous substances, facilitating their removal or transformation into less harmful forms.
Check Digit Verification of cas no
The CAS Registry Mumber 95037-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,3 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 95037-20:
(7*9)+(6*5)+(5*0)+(4*3)+(3*7)+(2*2)+(1*0)=130
130 % 10 = 0
So 95037-20-0 is a valid CAS Registry Number.
95037-20-0Relevant academic research and scientific papers
N-[2-amino-5-halo-6-(substituted)-3-pyrazinyl)-methylene]amine antimicrobial compounds
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, (2008/06/13)
Antimicrobial compounds of the formula: STR1 wherein: Hal is bromine or chlorine; R is halo; mono- or di-substituted mono- or diloweralkylamino wherein the loweralkyl substituents are hydroxy or loweralkanoyloxy; 4-morpholino; thiocyano; mercapto; straigh
3-Acyl-2-amino-5-halo-6-(substituted)pyrazine antimicrobial compounds
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, (2008/06/13)
Antimicrobial compounds of the formula: STR1 wherein: Hal is bromine or chlorine; R is chloro, but only when R1 is other than hydrogen; mono- or di-substituted mono- or diloweralkylamino wherein the loweralkyl substituents are hydroxy or loweralkanoyloxy; 4-morpholino; thiocyano; mercapto; straight or branched chain C1-8 alkylthio; mono- or di-substituted loweralkylthio wherein the substituents are hydroxy, amino, loweralkanoylamino, or loweralkoxycarbonyl; arylthio; loweralkylsulfoxy; or loweralkylsulfonyl; and R1 is hydrogen; straight or branched C1-8 alkyl; aryl; aryl substituted with up to two members selected from the group consisting of C1-3 alkyl, C1-3 alkoxy, halo, and mono- or di-C1-3 alkyl substituted amino; heteroaryl; formyl C2-4 alkenyl; or C2-4 alkenyl; are useful in various agricultural and industrial areas.
Pyrazine aldimine compounds as antimicrobial agents
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, (2008/06/13)
The instant invention is directed to a pyrazine compound represented by the formula STR1 wherein Z is --NH--, --NHSO2 --, --NHCO-- or --S--, Ar is a phenyl ring substituted by 1 or 2 substituents selected from the group consisting of halo, lower alkyl, lower alkoxy or nitro, and n is 0 or 1.
