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2-Chloromethyl-6-methoxy-4-methyl-pyridine is a trisubstituted pyridine-based building block, which is a heterocyclic ring base found in various biologically active compounds, such as vitamins niacin and pyridoxal. It plays a significant role in dehalogenation reactions and can also be utilized as a base in condensation reactions.

100636-47-3

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100636-47-3 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloromethyl-6-methoxy-4-methyl-pyridine is used as a building block for the synthesis of various biologically active compounds due to its trisubstituted pyridine structure. Its presence in many pharmaceutical compounds makes it a valuable component in drug development.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2-Chloromethyl-6-methoxy-4-methyl-pyridine is used as a key intermediate in the production of various organic compounds. Its ability to participate in dehalogenation reactions and act as a base in condensation reactions makes it a versatile component in creating complex molecules.
Used in Research and Development:
2-Chloromethyl-6-methoxy-4-methyl-pyridine is also utilized in research and development for the exploration of new chemical reactions and the creation of novel compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 100636-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,3 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 100636-47:
(8*1)+(7*0)+(6*0)+(5*6)+(4*3)+(3*6)+(2*4)+(1*7)=83
83 % 10 = 3
So 100636-47-3 is a valid CAS Registry Number.

100636-47-3Downstream Products

100636-47-3Relevant academic research and scientific papers

ELECTROPHILIC REACTION OF ALLYLTRIMETHYLSILANE WITH NITRILES IN THE PRESENCE OF BORON TRICHLORIDE

Hamana, Hiroshi,Sugasawa, Tsutomu

, p. 921 - 924 (2007/10/02)

Allyltrimethylsilane reacted with various nitriles in the presence of boron trichloride, giving after hydrolysis β,γ-unsaturated ketones in high yields.The reactions of substituted allyltrimethylsilanes and intramolecular reaction of allylic trimethylsilane with nitrile were also studied.

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