BF₄^(1-)*C₂₄H₃₀N₅OS⁽¹⁺⁾

Base Information

Chemical Name:BF₄^(1-)*C₂₄H₃₀N₅OS⁽¹⁺⁾
CAS No.:1219279-20-5
Molecular Formula:BF₄*C₂₄H₃₀N₅OS
Molecular Weight:523.406
Hs Code.:

BF<sub>4</sub><sup>(1-)</sup>*C<sub>24</sub>H<sub>30</sub>N<sub>5</sub>OS<sup>(1+)</sup>

Synonyms:BF₄^(1-)*C₂₄H₃₀N₅OS⁽¹⁺⁾

Suppliers and Price of BF₄^(1-)*C₂₄H₃₀N₅OS⁽¹⁺⁾

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
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price

Total 1 raw suppliers

Chemical Property of BF₄^(1-)*C₂₄H₃₀N₅OS⁽¹⁺⁾

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of BF₄^(1-)*C₂₄H₃₀N₅OS⁽¹⁺⁾

There total 7 articles about BF₄^(1-)*C₂₄H₃₀N₅OS⁽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:

: 1219277-79-8
BF₄^(1-)*C₂HF₃O₂*C₁₇H₂₅N₄O⁽¹⁺⁾

: 103-72-0
phenyl isothiocyanate

: 1219279-20-5
BF₄^(1-)*C₂₄H₃₀N₅OS⁽¹⁺⁾

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 80 ℃; for 8h; Inert atmosphere;
DOI:10.1080/00397910903013697

Reference yield:

: 1219277-15-2
C₂₀H₁₈N₃O₂⁽¹⁺⁾*Cl^(1-)

: 1219279-20-5
BF₄^(1-)*C₂₄H₃₀N₅OS⁽¹⁺⁾

Guidance literature:: Multi-step reaction with 5 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: dichloromethane / 0.5 h / 20 °C / Inert atmosphere

5: N-ethyl-N,N-diisopropylamine / acetonitrile / 8 h / 80 °C / Inert atmosphere

With sodium tetrafluoroborate; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide; In dichloromethane; acetonitrile;
DOI:10.1080/00397910903013697

Reference yield:

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

: 1219279-20-5
BF₄^(1-)*C₂₄H₃₀N₅OS⁽¹⁺⁾

Guidance literature:: Multi-step reaction with 4 steps

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

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

3: dichloromethane / 0.5 h / 20 °C / Inert atmosphere

4: N-ethyl-N,N-diisopropylamine / acetonitrile / 8 h / 80 °C / Inert atmosphere

With hydrazine hydrate; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide; In dichloromethane; acetonitrile;
DOI:10.1080/00397910903013697