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(S)-2-(2-(benzyloxy)-7-bromo-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethyl pivalate

Base Information
  • Chemical Name:(S)-2-(2-(benzyloxy)-7-bromo-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethyl pivalate
  • CAS No.:1403666-33-0
  • Molecular Formula:C26H32BrNO4S
  • Molecular Weight:534.514
  • Hs Code.:
(S)-2-(2-(benzyloxy)-7-bromo-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethyl pivalate

Synonyms:(S)-2-(2-(benzyloxy)-7-bromo-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethyl pivalate

Suppliers and Price of (S)-2-(2-(benzyloxy)-7-bromo-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethyl pivalate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 1 raw suppliers
Chemical Property of (S)-2-(2-(benzyloxy)-7-bromo-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethyl pivalate
Chemical Property:
Purity/Quality:

98% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (S)-2-(2-(benzyloxy)-7-bromo-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethyl pivalate

There total 9 articles about (S)-2-(2-(benzyloxy)-7-bromo-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethyl pivalate 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:
Guidance literature:
benzyl alcohol; With sodium hydride; at 20 ℃; for 0.5h;
(S)-2-(7-bromo-2-chloro-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethyl pivalate; at 60 ℃; for 0.75h;
Guidance literature:
Multi-step reaction with 5 steps
1.1: perchloric acid / 3.08 h / 0 - 20 °C
2.1: hydrogen / platinum on activated charcoal / ethyl acetate; ethanol / 5 h / 20 °C
3.1: acetic acid / tetrahydrofuran / 0.5 h / 0 °C
4.1: tert.-butylnitrite; copper dichloride / acetonitrile / 20 °C
5.1: sodium hydride / 0.5 h / 20 °C
5.2: 0.75 h / 60 °C
With tert.-butylnitrite; perchloric acid; hydrogen; sodium hydride; acetic acid; copper dichloride; platinum on activated charcoal; In tetrahydrofuran; ethanol; ethyl acetate; acetonitrile;
Guidance literature:
Multi-step reaction with 4 steps
1.1: hydrogen / platinum on activated charcoal / ethyl acetate; ethanol / 5 h / 20 °C
2.1: acetic acid / tetrahydrofuran / 0.5 h / 0 °C
3.1: tert.-butylnitrite; copper dichloride / acetonitrile / 20 °C
4.1: sodium hydride / 0.5 h / 20 °C
4.2: 0.75 h / 60 °C
With tert.-butylnitrite; hydrogen; sodium hydride; acetic acid; copper dichloride; platinum on activated charcoal; In tetrahydrofuran; ethanol; ethyl acetate; acetonitrile;
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