N,N-diisopropyl-2-methylbenzenecarbothioamide

Base Information

Chemical Name:N,N-diisopropyl-2-methylbenzenecarbothioamide
CAS No.:619314-47-5
Molecular Formula:C₁₄H₂₁NS
Molecular Weight:235.393
Hs Code.:

Synonyms:N,N-diisopropyl-2-methylbenzenecarbothioamide

Suppliers and Price of N,N-diisopropyl-2-methylbenzenecarbothioamide

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

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Chemical Property of N,N-diisopropyl-2-methylbenzenecarbothioamide

Chemical Property:

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Technology Process of N,N-diisopropyl-2-methylbenzenecarbothioamide

There total 3 articles about N,N-diisopropyl-2-methylbenzenecarbothioamide 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: 90.0%

: 6641-72-1
N,N-diisopropyl-2-methylbenzenecarboxamide

: 619314-47-5
N,N-diisopropyl-2-methylbenzenecarbothioamide

Guidance literature:: With Lawessons reagent; In various solvent(s); at 165 ℃; for 16h;
DOI:10.1002/ejoc.200300233

Reference yield:

: 933-88-0
ortho-toluoyl chloride

: 619314-47-5
N,N-diisopropyl-2-methylbenzenecarbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether / 16 h / 20 °C

2: 90 percent / Lawesson's reagent / various solvent(s) / 16 h / 165 °C

With Lawessons reagent; In diethyl ether;
DOI:10.1002/ejoc.200300233

Reference yield:

: 108-18-9
diisopropylamine

: 619314-47-5
N,N-diisopropyl-2-methylbenzenecarbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether / 16 h / 20 °C

2: 90 percent / Lawesson's reagent / various solvent(s) / 16 h / 165 °C

With Lawessons reagent; In diethyl ether;
DOI:10.1002/ejoc.200300233