(-)-(R)-N-[carbo-(1R)-menthoxy]-2,4,6-triisopropylbenzenesulfonimidoyl chloride

Base Information

Chemical Name:(-)-(R)-N-[carbo-(1R)-menthoxy]-2,4,6-triisopropylbenzenesulfonimidoyl chloride
CAS No.:253316-10-8
Molecular Formula:C₂₆H₄₂ClNO₃S
Molecular Weight:484.143
Hs Code.:

Synonyms:(-)-(R)-N-[carbo-(1R)-menthoxy]-2,4,6-triisopropylbenzenesulfonimidoyl chloride

Suppliers and Price of (-)-(R)-N-[carbo-(1R)-menthoxy]-2,4,6-triisopropylbenzenesulfonimidoyl chloride

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (-)-(R)-N-[carbo-(1R)-menthoxy]-2,4,6-triisopropylbenzenesulfonimidoyl chloride

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (-)-(R)-N-[carbo-(1R)-menthoxy]-2,4,6-triisopropylbenzenesulfonimidoyl chloride

There total 2 articles about (-)-(R)-N-[carbo-(1R)-menthoxy]-2,4,6-triisopropylbenzenesulfonimidoyl chloride 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: 36.0%

: 117659-09-3
2,4,6-triisopropylbenzenesulfinyl chloride

: 52719-92-3
(-)-Menthyl-N-p-nitrobenzolsulfonoxycarbamat

: 253316-10-8
(-)-(R)-N-[carbo-(1R)-menthoxy]-2,4,6-triisopropylbenzenesulfonimidoyl chloride

Guidance literature:: With triethylamine; In toluene; at 20 ℃;
DOI:10.1080/10426509908037031

Reference yield:

: 18099-26-8
2,4,6-triisopropyl-benzenesulfinic acid

: 253316-10-8
(-)-(R)-N-[carbo-(1R)-menthoxy]-2,4,6-triisopropylbenzenesulfonimidoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / 2 h / 25 °C

2: 36 percent / Et₃N / toluene / 20 °C

With thionyl chloride; triethylamine; In toluene; 1: Chlorination / 2: Substitution;
DOI:10.1080/10426509908037031