C₃₆H₆₀N₆O₇*ClH

Base Information

Chemical Name:C₃₆H₆₀N₆O₇*ClH
CAS No.:1356203-91-2
Molecular Formula:C₃₆H₆₀N₆O₇*ClH
Molecular Weight:725.369
Hs Code.:

C<sub>36</sub>H<sub>60</sub>N<sub>6</sub>O<sub>7</sub>*ClH

Synonyms:

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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 C₃₆H₆₀N₆O₇*ClH

Chemical Property:

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Technology Process of C₃₆H₆₀N₆O₇*ClH

There total 8 articles about C₃₆H₆₀N₆O₇*ClH 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:

: 869795-62-0
H-MeLeu-Ala-OBn hydrochloride

: 1356203-91-2
C₃₆H₆₀N₆O₇*ClH

Guidance literature:: Multi-step reaction with 6 steps

1: tert-butylisonitrile / chloroform / 23 °C / Inert atmosphere

2: hydrogenchloride / 1,4-dioxane / 0.17 h

3: Cyclohexyl isocyanide / chloroform / 23 °C / Inert atmosphere

4: hydrogenchloride / 1,4-dioxane / 0.17 h

5: Cyclohexyl isocyanide / chloroform / 0.75 h / 80 °C / Inert atmosphere; Microwave irradiation

6: hydrogenchloride / 1,4-dioxane / 0.17 h

With hydrogenchloride; Cyclohexyl isocyanide; tert-butylisonitrile; In 1,4-dioxane; chloroform;
DOI:10.1021/ja2103372

Reference yield:

: 5557-81-3,5557-83-5,34404-37-0
(R)-benzyl 2-aminopropanoate hydrochloride

: 1356203-91-2
C₃₆H₆₀N₆O₇*ClH

Guidance literature:: Multi-step reaction with 8 steps

1: tert-butylisonitrile / chloroform / 23 °C / Inert atmosphere

2: hydrogenchloride / 1,4-dioxane / 0.17 h

3: tert-butylisonitrile / chloroform / 23 °C / Inert atmosphere

4: hydrogenchloride / 1,4-dioxane / 0.17 h

5: Cyclohexyl isocyanide / chloroform / 23 °C / Inert atmosphere

6: hydrogenchloride / 1,4-dioxane / 0.17 h

7: Cyclohexyl isocyanide / chloroform / 0.75 h / 80 °C / Inert atmosphere; Microwave irradiation

8: hydrogenchloride / 1,4-dioxane / 0.17 h

With hydrogenchloride; Cyclohexyl isocyanide; tert-butylisonitrile; In 1,4-dioxane; chloroform;
DOI:10.1021/ja2103372

Reference yield:

: 81135-26-4
N-(tert-butoxycarbonyl)-L-valyl-N-methyl-L-leucyl-L-alanine benzyl ester

: 1356203-91-2
C₃₆H₆₀N₆O₇*ClH

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogenchloride / 1,4-dioxane / 0.17 h

2: Cyclohexyl isocyanide / chloroform / 23 °C / Inert atmosphere

3: hydrogenchloride / 1,4-dioxane / 0.17 h

4: Cyclohexyl isocyanide / chloroform / 0.75 h / 80 °C / Inert atmosphere; Microwave irradiation

5: hydrogenchloride / 1,4-dioxane / 0.17 h

With hydrogenchloride; Cyclohexyl isocyanide; In 1,4-dioxane; chloroform;
DOI:10.1021/ja2103372