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Pyrimidine, 5-iodo-4-methoxy-2-methyl-6-(trifluoromethyl)is a pyrimidine derivative with a molecular formula C8H6F3IN2O. It is a chemical compound commonly used in organic synthesis and pharmaceutical research. Known for its unique chemical and biological properties, Pyrimidine, 5-iodo-4-methoxy-2-methyl-6-(trifluoromethyl)- has potential applications in the development of drugs and agrochemicals.

792934-97-5

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792934-97-5 Usage

Uses

Used in Pharmaceutical Research:
Pyrimidine, 5-iodo-4-methoxy-2-methyl-6-(trifluoromethyl)is used as a building block in the synthesis of various biologically active molecules. Its unique properties make it a promising candidate for the development of drugs with anti-inflammatory, anti-tumor, and anti-viral activities.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Pyrimidine, 5-iodo-4-methoxy-2-methyl-6-(trifluoromethyl)is used as a pharmacophore in the design of novel therapeutic agents. Its potential to contribute to the development of new drugs makes it an important compound for research and development in this industry.

Check Digit Verification of cas no

The CAS Registry Mumber 792934-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,2,9,3 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 792934-97:
(8*7)+(7*9)+(6*2)+(5*9)+(4*3)+(3*4)+(2*9)+(1*7)=225
225 % 10 = 5
So 792934-97-5 is a valid CAS Registry Number.

792934-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-iodo-4-methoxy-2-methyl-6-(trifluoromethyl)pyrimidine

1.2 Other means of identification

Product number -
Other names -

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:792934-97-5 SDS

792934-97-5Relevant academic research and scientific papers

Fungicidal pyrimidine derivatives

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, (2008/06/13)

Fungicidal pyrimidine derivatives and the use as a fungicide of the compounds of formula (1): wherein R1 is H, C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3-C6cycloalkyl, C1-C6alkoxy, C3-C6cycloalkoxy, C1-C6alkylthio, C1-C6alkylsulfinyl, C1-C6alkylsulfonyl, phenyl, pyridinyl or azolyl groups, (being optionally substituted by one or more substituents); or N(R4)C(O)R5, R2 is polyfluoroalkyl, R3 is fluorine, chlorine, bromine or iodine; ethenyl or ethynyl (being optionally substituted by one or more of halogen), R4 and R5 are, independently, H, C1-C6alkyl, C2-C6alkenyl or C2-C6alkynyl groups, (being optionally substituted by one or more of halogen or cyano); or R4 and R5 can join together to form a 5 or 6-membered ring, Q is a heteroaromatic ring selected from the following ring system; imidazol-1-yl, pyrazol-1-yl, 1,2,3-triazol-1-yl, 1,2,3-triazol-2-yl, 1,2,4-triazol-1-yl, 1,2,4-triazol-4-yl, benzimidazol-1-yl or tetrazol-5-yl groups, (being optionally substituted by one or more of substituents).

Fungicidal pyrimidine derivatives

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Page column 14, (2010/02/09)

Fungicidal pyrimidine derivatives and the use as a fungicide of the compounds of formula (1): wherein R1is H, C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl C3-C6cycloalkyl, C1-C6alkoxy, C3-C6cycloalkoxy, C1-C6alylthio, C1-C6alkylsulfinyl, C1-C6alkylsulfonyl, phenyl, pyridinyl or azolyl groups, (being optionally substituted by one or more substituents); or N(R4)C(O)R5, R2is polyfluoroalkyl, R3is fluorine, chlorine, bromine or iodine; ethenyl or ethynyl (being optionally substituted by one or more of halogen), R4and R5are, independently, H, C1-C6alkyl, C2-C6alkenyl or C2-C6alkynyl groups, (being optionally substituted by one or more of halogen or cyano); or R4and R5can join together to form a 5 or 6-membered ring, Q is a heteroaromatic ring selected from the following ring system; imidazol-1-yl, pyrazol-1-yl, 1,2,3-triazol-1-yl, 1,2,3-triazol-2-yl, 1,2,4-triazol-1-yl, 1,2,4-triazol-1-yl, benzimidazol-1-yl or tetrazol-5-yl groups, (being optionally substituted by one or more of substituents).

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