936644-43-8

Basic information

• Product Name: {(R,R)-2-[2-(4-tert-butylcyclohexa-1,4-dienyl)-ethanesulfonylamino]-1,2-diphenylethyl}-tert-butyl carbamate
• CAS NO: 936644-43-8
• Molecular Weight: 538.751
• Mol File: 936644-43-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: {(R,R)-2-[2-(4-tert-butylcyclohexa-1,4-dienyl)-ethanesulfonylamino]-1,2-diphenylethyl}-tert-butyl carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: {(R,R)-2-[2-(4-tert-butylcyclohexa-1,4-dienyl)-ethanesulfonylamino]-1,2-diphenylethyl}-tert-butyl carbamate(936644-43-8)
• EPA Substance Registry System: {(R,R)-2-[2-(4-tert-butylcyclohexa-1,4-dienyl)-ethanesulfonylamino]-1,2-diphenylethyl}-tert-butyl carbamate(936644-43-8)

Safety Data

• Hazardous Substances Data: 936644-43-8(Hazardous Substances Data)

Upstream product

• 35132-20-8 (R,R)-1,2-diphenylethylenediamine 
• 3732-61-4 3,4,4-trimethyl-1-penten-3-ol 
• 936644-41-6 [(R,R)-2-(but-3-yne-1-sulfonylamino)-1,2-diphenylethyl]-tert-butyl carbamate 
• 2495-32-1 4,4-dimethyl-3-methylenepent-1-ene 
• 936644-40-5 but-3-yne-1-sulfonic acid ((R,R)-2-amino-1,2-diphenylethyl)-amide 

Relevant articles and documents

The use of a [4 + 2] cycloaddition reaction for the preparation of a series of 'tethered' Ru(ii)-diamine and aminoalcohol complexes

A series of catalysts have been prepared for use in the asymmetric transfer hydrogenation of ketones. The complexes were prepared using a [4 + 2] cycloaddition reaction at a key step in the reaction sequence. This provides a means for the synthesis of cat