6-(4-iodobenzenesulfonamido)hexanoic acid 6(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)hex-5-enyl ester

Base Information

Chemical Name:6-(4-iodobenzenesulfonamido)hexanoic acid 6(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)hex-5-enyl ester
CAS No.:1447810-97-0
Molecular Formula:C₂₄H₃₇BINO₆S
Molecular Weight:605.342
Hs Code.:

Synonyms:6-(4-iodobenzenesulfonamido)hexanoic acid 6(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)hex-5-enyl ester

Suppliers and Price of 6-(4-iodobenzenesulfonamido)hexanoic acid 6(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)hex-5-enyl ester

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 6-(4-iodobenzenesulfonamido)hexanoic acid 6(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)hex-5-enyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 6-(4-iodobenzenesulfonamido)hexanoic acid 6(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)hex-5-enyl ester

There total 7 articles about 6-(4-iodobenzenesulfonamido)hexanoic acid 6(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)hex-5-enyl ester 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: 27.0%

: 172264-25-4
(E)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hex-5-en-1-ol

: 1094668-77-5
6-(4-iodobenzenesulfonamido)hexanoic acid

: 1447810-97-0
6-(4-iodobenzenesulfonamido)hexanoic acid 6(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)hex-5-enyl ester

Guidance literature:: With dmap; diisopropyl-carbodiimide; In dichloromethane; at 0 - 20 ℃; for 12h;
DOI:10.1039/c3ob41020j

Reference yield:

: 73448-13-2
tert-butyldimethylsilyl hex-5-yn-1-yl ether

: 1447810-97-0
6-(4-iodobenzenesulfonamido)hexanoic acid 6(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)hex-5-enyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: tetrahydrofuran / 6 h / 75 °C

1.2: 1 h / 20 °C

2.1: dmap; diisopropyl-carbodiimide / dichloromethane / 12 h / 0 - 20 °C

With dmap; diisopropyl-carbodiimide; In tetrahydrofuran; dichloromethane;
DOI:10.1039/c3ob41020j

Reference yield:

: 928-90-5
5-hexyl-1-ol

: 1447810-97-0
6-(4-iodobenzenesulfonamido)hexanoic acid 6(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)hex-5-enyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine; dmap / dichloromethane / 26 h / 0 - 20 °C

2.1: tetrahydrofuran / 6 h / 75 °C

2.2: 1 h / 20 °C

3.1: dmap; diisopropyl-carbodiimide / dichloromethane / 12 h / 0 - 20 °C

With dmap; triethylamine; diisopropyl-carbodiimide; In tetrahydrofuran; dichloromethane;
DOI:10.1039/c3ob41020j