p-(Adamant-1-ylcarbamoyl)-N-(carboxypentamethylen)benzamidiniumchlorid

Base Information

Chemical Name:p-(Adamant-1-ylcarbamoyl)-N-(carboxypentamethylen)benzamidiniumchlorid
CAS No.:80626-05-7
Molecular Formula:C₂₄H₃₃N₃O₃*ClH
Molecular Weight:448.005
Hs Code.:

Synonyms:p-(Adamant-1-ylcarbamoyl)-N-(carboxypentamethylen)benzamidiniumchlorid

Suppliers and Price of p-(Adamant-1-ylcarbamoyl)-N-(carboxypentamethylen)benzamidiniumchlorid

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
Packaging
price

Total 0 raw suppliers

Chemical Property of p-(Adamant-1-ylcarbamoyl)-N-(carboxypentamethylen)benzamidiniumchlorid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of p-(Adamant-1-ylcarbamoyl)-N-(carboxypentamethylen)benzamidiniumchlorid

There total 4 articles about p-(Adamant-1-ylcarbamoyl)-N-(carboxypentamethylen)benzamidiniumchlorid 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: 28.0%

: 70180-88-0
p-(Adamant-1-ylcarbamoyl)benzimidsaeureethylesterhydrochlorid

: 60-32-2,93208-38-9
6-aminohexanoic acid

: 80626-05-7
p-(Adamant-1-ylcarbamoyl)-N-(carboxypentamethylen)benzamidiniumchlorid

Guidance literature:: With trimethylamine; In ethanol; at 65 ℃; for 3h; Heating;

Reference yield:

: 6068-72-0
4-cyanobenzoyl chlorIde

: 80626-05-7
p-(Adamant-1-ylcarbamoyl)-N-(carboxypentamethylen)benzamidiniumchlorid

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / 1,2-dichloro-benzene / 1 h / 160 °C / Heating

2: 90 percent / 10 mol/l HCl/EtOH / ethanol; CHCl₃ / 144 h / 4 °C

3: 28 percent / N(CH₃)3, / ethanol / 3 h / 65 °C / Heating

With hydrogenchloride; ethanol; trimethylamine; In ethanol; chloroform; 1,2-dichloro-benzene;

Reference yield:

: 665-66-7,13878-11-0
amantadine hydrochloride

: 80626-05-7
p-(Adamant-1-ylcarbamoyl)-N-(carboxypentamethylen)benzamidiniumchlorid

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / 1,2-dichloro-benzene / 1 h / 160 °C / Heating

2: 90 percent / 10 mol/l HCl/EtOH / ethanol; CHCl₃ / 144 h / 4 °C

3: 28 percent / N(CH₃)3, / ethanol / 3 h / 65 °C / Heating

With hydrogenchloride; ethanol; trimethylamine; In ethanol; chloroform; 1,2-dichloro-benzene;