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36936-23-9
5-Chloro-6-methylpyridin-2-amine

Catalog#:1P003N50

CAS:36936-23-9

MDL:MFCD09453335

Molecular Formula:C6H7ClN2

Molecular Weight:142.5862

UN Number:

Haz Class:

Packing Group:

Synonyms: 5-chloro-6-methylpyridin-2-amine; 36936-23-9; AK-53663; PubChem5718; SCHEMBL558598; 6-Amino-3-chloro-2-picoline; 5-chloro-6-methyl-pyridineamine; CTK8B6113; DTXSID50482438; SHIKRPPKGCWKJO-UHFFFAOYSA-N; BCP27113; ZX-CM006439; 2-AMINO-5-CHLORO-6-METHYLPYRIDINE; ANW-52614; CC-002; FCH868776; RW3366; STL119698; ZINC15423947; AKOS000108170; AB50593; AS04695; CS-W003618; 2-Amino-5-chloro-6-picoline; MCULE-1256126142; QC-2174; TRA0097374; AJ-67311; AS-18950; OR345085; SY021462; 2-Amino-5-chloro-6-methylpyridine, 97%; 6-AMINO-3-CHLORO-2-METHYLPYRIDINE; AB0031042; 5-CHLORO-6-METHYL-2-PYRIDINAMINE; AB1007755; AX8070401; TC-063073; AM20051120; BB 0244530; FT-0651910; X3365; 2-Amino-5-chloro-6-methylpyridine, AldrichCPR; Y-5284; Z-8105; 6-Amino-3-chloropicoline; MFCD09453335 (97+%); I02-1364; 6-Amino-3-chloropicolline; 5-Chloro-6-methylpyridin-2-amine; 5-Chloro-6-methyl-2-pyridinamine; C6H7ClN2; ACN-026907; A2920; A15532; (1-(5-CARBOXYPENTYL)-3,3-DIMETHYL-3H-INDOL-1-IUM-2-YL)METHANIDE HYDROBROMIDE; 16108-03-5; 2-Amino-5-Chloro-6-Methyl Pyridine; 2-Pyridinamine, 5-chloro-6-methyl-; 5-Chloro-6-methyl-pyridin-2-ylamine; MFCD09453335;

Keywords: 36936-23-9,MFCD09453335,1P003N50,5-Chloro-6-methylpyridin-2-amine,C6H7ClN2

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Catalog# Purity Size Price Dis. Price Availability Quantity
1P003N50 97% 250mg $7.00 $5.00 In Stock USA ADD TO CART BUY NOW
1P003N50 97% 1g $16.00 $12.00 In Stock USA ADD TO CART BUY NOW
1P003N50 97% 5g $68.00 $51.00 In Stock USA ADD TO CART BUY NOW
1P003N50 97% 10g $109.00 $82.00 In Stock USA ADD TO CART BUY NOW
1P003N50 97% 25g $216.00 $162.00 In Stock USA ADD TO CART BUY NOW

  • 5-Chloro-6-methylpyridin-2-amine, also known as $name$, is a key building block in chemical synthesis with versatile applications. This compound serves as a crucial intermediate in the pharmaceutical industry, specifically in the development of various drugs and active pharmaceutical ingredients (APIs). Its unique structure and reactivity make it a valuable tool for organic chemists.In organic synthesis, 5-Chloro-6-methylpyridin-2-amine can be utilized in the creation of diverse chemical compounds through functional group transformations. Its amino and chloro substituents allow for selective modifications, enabling the introduction of various functional groups at specific positions in the molecule. This flexibility is essential for designing and crafting complex organic molecules with desired properties.Furthermore, 5-Chloro-6-methylpyridin-2-amine can participate in key reactions such as nucleophilic substitution, Suzuki coupling, and reductive amination. These reactions open up opportunities for the synthesis of biologically active compounds, intermediates for agrochemicals, and materials for various industrial applications. Its role as a synthetic building block highlights its importance in driving innovation and discovery in the field of organic chemistry.

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