1-tert-butyl 5-methyl 2-(diphenylmethylenediamino)-4-isobutylpentanedioate

Base Information

Chemical Name:1-tert-butyl 5-methyl 2-(diphenylmethylenediamino)-4-isobutylpentanedioate
CAS No.:1067977-45-0
Molecular Formula:C₂₇H₃₅NO₄
Molecular Weight:437.579
Hs Code.:

Synonyms:1-tert-butyl 5-methyl 2-(diphenylmethylenediamino)-4-isobutylpentanedioate

Suppliers and Price of 1-tert-butyl 5-methyl 2-(diphenylmethylenediamino)-4-isobutylpentanedioate

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 1-tert-butyl 5-methyl 2-(diphenylmethylenediamino)-4-isobutylpentanedioate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-tert-butyl 5-methyl 2-(diphenylmethylenediamino)-4-isobutylpentanedioate

There total 1 articles about 1-tert-butyl 5-methyl 2-(diphenylmethylenediamino)-4-isobutylpentanedioate 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:

: 3070-69-7
methyl 2-(2-methylpropyl)acrylate

: 81477-94-3
N-(diphenylmethylene)glycine tert-butyl ester

: 1067977-39-2
1-tert-butyl 5-methyl 2-(diphenylmethylenediamino)-4-isobutylpentanedioate

: 1067977-45-0
1-tert-butyl 5-methyl 2-(diphenylmethylenediamino)-4-isobutylpentanedioate

: 1-tert-butyl 5-methyl 2-(diphenylmethylenediamino)-4-isobutylpentanedioate

Guidance literature:: With calcium bis-iso-propoxide; (S,S)-2,2'-methylenebis(4-phenyl-2-oxazoline); In tetrahydrofuran; at -30 ℃; for 12h; optical yield given as %ee; enantioselective reaction; Molecular sieve;
DOI:10.1021/ja8032058