6-<<<-2-cyclohexen-1-yl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide

Base Information

Chemical Name:6-<<<-2-cyclohexen-1-yl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide
CAS No.:131906-70-2
Molecular Formula:Br*C₃₅H₅₁N₂O₅S
Molecular Weight:691.77
Hs Code.:

6-<<<<cis-6-benzoyl-cis-4-<(4-hexylphenyl)sulfonyl>-2-cyclohexen-1-yl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide

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Suppliers and Price of 6-<<<-2-cyclohexen-1-yl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide

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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 6-<<<-2-cyclohexen-1-yl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide

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Technology Process of 6-<<<-2-cyclohexen-1-yl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide

There total 1 articles about 6-<<<-2-cyclohexen-1-yl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide 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:

: 131906-60-0
(E,E)-6-<<<<4-<(4-hexylphenyl)sulfonyl>-1,3-butadienyl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide

: 768-03-6,26742-84-7
Phenyl vinyl ketone

: 131906-64-4
6-<<<-2-cyclohexen-1-yl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide

: 131906-70-2
6-<<<-2-cyclohexen-1-yl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide

Guidance literature:: In water; at 50 ℃; for 10h; Product distribution; influence of micelle aggregation on regiochemistry; other times, other solvents, or with hexadecyltrimethylammonium bromide, other dienophile, other 1,3-butadienyl carbamates;
DOI:10.1021/jo00007a041