2--4-chloro-6-methylpyrimidine

Base Information

Chemical Name:2--4-chloro-6-methylpyrimidine
CAS No.:74246-40-5
Molecular Formula:C₁₅H₁₈ClN₃
Molecular Weight:275.781
Hs Code.:

2-<N-(p-n-Butylanilino)>-4-chloro-6-methylpyrimidine

Synonyms:2--4-chloro-6-methylpyrimidine

Suppliers and Price of 2--4-chloro-6-methylpyrimidine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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price

Total 1 raw suppliers

Chemical Property of 2--4-chloro-6-methylpyrimidine

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

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Technology Process of 2--4-chloro-6-methylpyrimidine

There total 4 articles about 2--4-chloro-6-methylpyrimidine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 61.0%

: 74246-39-2
2--6-methyl-4(3H)-pyrimidinone

: 74246-40-5
2--4-chloro-6-methylpyrimidine

Guidance literature:: With trichlorophosphate; for 2h; Heating;
DOI:10.1007/BF02401734

Reference yield:

: 53736-37-1
2-nitroamino-4(3H)-pyrimidinone

: 74246-40-5
2--4-chloro-6-methylpyrimidine

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / butan-1-ol / 3 h / Heating

2: 61 percent / POCl₃ / 2 h / Heating

With trichlorophosphate; In butan-1-ol;
DOI:10.1007/BF02401734

Reference yield:

: 104-13-2
4-Butylaniline

: 74246-40-5
2--4-chloro-6-methylpyrimidine

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / butan-1-ol / 3 h / Heating

2: 61 percent / POCl₃ / 2 h / Heating

With trichlorophosphate; In butan-1-ol;
DOI:10.1007/BF02401734