Benzylideneamine

Base Information

Chemical Name:Benzylideneamine
CAS No.:123016-86-4
Molecular Formula:C₁₄H₂₅NSi₂
Molecular Weight:263.53
Hs Code.:

Benzylidene<bis(trimethylsilyl)methyl>amine

Synonyms:Benzylideneamine

Suppliers and Price of Benzylideneamine

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 Benzylideneamine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Benzylideneamine

There total 4 articles about Benzylideneamine 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: 34.0%

: 100-52-7
benzaldehyde

: 171414-56-5
Bis(trimethylsilyl)methyl isocyanate

: 123016-86-4
Benzylideneamine

: 5-Phenyl-4-(trimethylsilyl)oxazolidin-2-one

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at -15 ℃; for 0.25h;
DOI:10.1021/jo00124a011

Reference yield:

: 134340-01-5
bis(trimethylsilyl)methyl azide

: 123016-86-4
Benzylideneamine

Guidance literature:: Multi-step reaction with 3 steps

1: tetrahydrofuran / 2 h / 25 °C

2: diethyl ether / 0.08 h / 25 °C

3: 12 percent / TBAF / tetrahydrofuran / 0.25 h / -15 °C

With tetrabutyl ammonium fluoride; In tetrahydrofuran; diethyl ether;
DOI:10.1021/jo00124a011

Reference yield:

: 171414-55-4
<imino>triphenylphosphorane

: 123016-86-4
Benzylideneamine

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether / 0.08 h / 25 °C

2: 12 percent / TBAF / tetrahydrofuran / 0.25 h / -15 °C

With tetrabutyl ammonium fluoride; In tetrahydrofuran; diethyl ether;
DOI:10.1021/jo00124a011