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C16H17N3OSi

Base Information Edit
C<sub>16</sub>H<sub>17</sub>N<sub>3</sub>OSi

Synonyms:C16H17N3OSi

Suppliers and Price of C16H17N3OSi
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C16H17N3OSi Edit
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Technology Process of C16H17N3OSi

There total 4 articles about C16H17N3OSi 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:
With camphor-10-sulfonic acid; In methanol; for 1h;
DOI:10.1016/j.tetlet.2013.07.001
Guidance literature:
C16H16OSi; With (1R,2R) N,N′-bis(3,5-di-tertbutylsalicylidene)-1,2-cyclohexanediamino chromium(III) chloride; In diethyl ether; at 20 ℃; for 0.25h;
trimethylsilylazide; In diethyl ether; Overall yield = 59 %; enantioselective reaction;
DOI:10.1016/j.tetlet.2013.07.001
Guidance literature:
Multi-step reaction with 2 steps
1: (1R,2R) N,N′-bis(3,5-di-tertbutylsalicylidene)-1,2-cyclohexanediamino chromium(III) chloride / diethyl ether / 0.25 h / -70 °C
2: (1R,2R) N,N′-bis(3,5-di-tertbutylsalicylidene)-1,2-cyclohexanediamino chromium(III) chloride / diethyl ether / 0.25 h / 20 °C
With (1R,2R) N,N′-bis(3,5-di-tertbutylsalicylidene)-1,2-cyclohexanediamino chromium(III) chloride; In diethyl ether;
DOI:10.1016/j.tetlet.2013.07.001
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