BF₄^(1-)*C₁₇H₂₅N₄O⁽¹⁺⁾

Base Information

Chemical Name:BF₄^(1-)*C₁₇H₂₅N₄O⁽¹⁺⁾
CAS No.:1219277-78-7
Molecular Formula:BF₄*C₁₇H₂₅N₄O
Molecular Weight:388.216
Hs Code.:

BF<sub>4</sub><sup>(1-)</sup>*C<sub>17</sub>H<sub>25</sub>N<sub>4</sub>O<sup>(1+)</sup>

Synonyms:

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Chemical Property of BF₄^(1-)*C₁₇H₂₅N₄O⁽¹⁺⁾

Chemical Property:

Purity/Quality:

Safty Information:

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Technology Process of BF₄^(1-)*C₁₇H₂₅N₄O⁽¹⁺⁾

There total 6 articles about BF₄^(1-)*C₁₇H₂₅N₄O⁽¹⁺⁾ 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:

: 1219277-23-2
BF₄^(1-)*C₂₀H₁₈N₃O₂⁽¹⁺⁾

: 1219277-78-7
BF₄^(1-)*C₁₇H₂₅N₄O⁽¹⁺⁾

Guidance literature:: Multi-step reaction with 3 steps

1: hydrazine hydrate / acetonitrile / 8 h / 80 °C

2: diisopropyl-carbodiimide / acetonitrile / 8 h / 20 °C / Inert atmosphere

3: trifluoroacetic acid / dichloromethane

With hydrazine hydrate; trifluoroacetic acid; diisopropyl-carbodiimide; In dichloromethane; acetonitrile;
DOI:10.1080/00397910903013697

Reference yield:

: 1219277-15-2
C₂₀H₁₈N₃O₂⁽¹⁺⁾*Cl^(1-)

: 1219277-78-7
BF₄^(1-)*C₁₇H₂₅N₄O⁽¹⁺⁾

Guidance literature:: Multi-step reaction with 4 steps

1: sodium tetrafluoroborate / acetonitrile / 72 h / 80 °C

2: hydrazine hydrate / acetonitrile / 8 h / 80 °C

3: diisopropyl-carbodiimide / acetonitrile / 8 h / 20 °C / Inert atmosphere

4: trifluoroacetic acid / dichloromethane

With sodium tetrafluoroborate; hydrazine hydrate; trifluoroacetic acid; diisopropyl-carbodiimide; In dichloromethane; acetonitrile;
DOI:10.1080/00397910903013697

Reference yield:

: 1219277-28-7
BF₄^(1-)*C₁₂H₁₆N₃⁽¹⁺⁾

: 1219277-78-7
BF₄^(1-)*C₁₇H₂₅N₄O⁽¹⁺⁾

Guidance literature:: Multi-step reaction with 2 steps

1: diisopropyl-carbodiimide / acetonitrile / 8 h / 20 °C / Inert atmosphere

2: trifluoroacetic acid / dichloromethane

With trifluoroacetic acid; diisopropyl-carbodiimide; In dichloromethane; acetonitrile;
DOI:10.1080/00397910903013697