Ethyl (1)-7-amino-8-methylnonan-1-oate

Base Information

Chemical Name:Ethyl (1)-7-amino-8-methylnonan-1-oate
CAS No.:64877-79-8
Molecular Formula:C₁₂H₂₅NO₂
Molecular Weight:215.336
Hs Code.:
European Community (EC) Number:265-261-7
DSSTox Substance ID:DTXSID901304872

Synonyms:Ethyl (1)-7-amino-8-methylnonan-1-oate;EINECS 265-261-7;64877-79-8;AARWQBUFJFZTFS-UHFFFAOYSA-N;DTXSID901304872;ETHYL 7-AMINO-8-METHYLNONANOATE

Suppliers and Price of Ethyl (1)-7-amino-8-methylnonan-1-oate

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 5 raw suppliers

Chemical Property of Ethyl (1)-7-amino-8-methylnonan-1-oate

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:9
Exact Mass:215.188529040
Heavy Atom Count:15
Complexity:169

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)CCCCCC(C(C)C)N

Technology Process of Ethyl (1)-7-amino-8-methylnonan-1-oate

There total 5 articles about Ethyl (1)-7-amino-8-methylnonan-1-oate 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:

: 126245-80-5
ethyl 8-methyl-7-oxononanoate

: 64877-79-8,64877-80-1,64877-83-4
ethyl 7-amino-8-methylnonanoate

Guidance literature:: Multi-step reaction with 4 steps

1: 85 percent / N-bromosuccinimide / CCl₄ / 5 h / Heating

2: 55 percent / lithium bromide / dimethylformamide / 1 h / 95 °C

3: 75 percent / hydroxylammonium chloride / ethanol / 5 h / Heating

4: zinc powder, acetic acid / Ambient temperature

With N-Bromosuccinimide; hydroxylamine hydrochloride; acetic acid; lithium bromide; zinc; In tetrachloromethane; ethanol; N,N-dimethyl-formamide;

Reference yield:

: 126245-82-7
ethyl 8-methyl-7-oxo-8-nonenoate

: 64877-79-8,64877-80-1,64877-83-4
ethyl 7-amino-8-methylnonanoate

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / hydroxylammonium chloride / ethanol / 5 h / Heating

2: zinc powder, acetic acid / Ambient temperature

With hydroxylamine hydrochloride; acetic acid; zinc; In ethanol;

Reference yield:

: 126245-81-6
ethyl 8-bromo-8-methyl-7-oxononanoate

: 64877-79-8,64877-80-1,64877-83-4
ethyl 7-amino-8-methylnonanoate

Guidance literature:: Multi-step reaction with 3 steps

1: 55 percent / lithium bromide / dimethylformamide / 1 h / 95 °C

2: 75 percent / hydroxylammonium chloride / ethanol / 5 h / Heating

3: zinc powder, acetic acid / Ambient temperature

With hydroxylamine hydrochloride; acetic acid; lithium bromide; zinc; In ethanol; N,N-dimethyl-formamide;