3,6-bis(5-broMo-4-(2-ethylhexyl)thiophen-2-yl)-1,2,4,5-tetrazine

Base Information

Chemical Name:3,6-bis(5-broMo-4-(2-ethylhexyl)thiophen-2-yl)-1,2,4,5-tetrazine
CAS No.:1260224-09-6
Molecular Formula:C₂₆H₃₆Br₂N₄S₂
Molecular Weight:628.539
Hs Code.:
Mol file:1260224-09-6.mol

Synonyms:3,6-bis(5-broMo-4-(2-ethylhexyl)thiophen-2-yl)-1,2,4,5-tetrazine

Suppliers and Price of 3,6-bis(5-broMo-4-(2-ethylhexyl)thiophen-2-yl)-1,2,4,5-tetrazine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 8 raw suppliers

Chemical Property of 3,6-bis(5-broMo-4-(2-ethylhexyl)thiophen-2-yl)-1,2,4,5-tetrazine

Chemical Property:

PSA：108.04000
LogP:9.76640

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

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Technology Process of 3,6-bis(5-broMo-4-(2-ethylhexyl)thiophen-2-yl)-1,2,4,5-tetrazine

There total 6 articles about 3,6-bis(5-broMo-4-(2-ethylhexyl)thiophen-2-yl)-1,2,4,5-tetrazine 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: 46.0%

: 1260224-08-5
3,6-bis[4-(2-ethylhexyl)thien-2-yl]-s-tetrazine

: 1260224-09-6
3,6-bis[5-bromo-4-(2-ethylhexyl)thien-2-yl]-s-tetrazine

Guidance literature:: With N-Bromosuccinimide; acetic acid; In chloroform; at 20 - 80 ℃;
DOI:10.1039/c0cc02766a

Reference yield:

: C₂₆H₄₀N₄S₂

: 1260224-09-6
3,6-bis[5-bromo-4-(2-ethylhexyl)thien-2-yl]-s-tetrazine

Guidance literature:: Multi-step reaction with 2 steps

1: isopentyl nitrite / chloroform / 20 °C

2: N-Bromosuccinimide; acetic acid / chloroform / 80 °C

With N-Bromosuccinimide; acetic acid; isopentyl nitrite; In chloroform;
DOI:10.1021/cm200330c

Reference yield:

: 1260224-06-3
4-(2-ethylhexyl)-2-thiophenecarbaldehyde

: 1260224-09-6
3,6-bis[5-bromo-4-(2-ethylhexyl)thien-2-yl]-s-tetrazine

Guidance literature:: Multi-step reaction with 5 steps

1: pyridine; hydroxylamine hydrochloride / ethanol / 80 °C

2: potassium acetate / acetic anhydride / 150 °C

3: sulfur; hydrazine hydrate / ethanol / 20 °C / Reflux

4: isopentyl nitrite / chloroform / 20 °C

5: N-Bromosuccinimide; acetic acid / chloroform / 80 °C

With pyridine; N-Bromosuccinimide; hydroxylamine hydrochloride; potassium acetate; sulfur; hydrazine hydrate; acetic acid; isopentyl nitrite; In ethanol; chloroform; acetic anhydride; 3: Pinner amidine synthesis;
DOI:10.1021/cm200330c