106729-74-2

Basic information

• Product Name: 1,2-cis-2,3-trans-2-benzamido-3-bromocyclohexyl benzoate
• CAS NO: 106729-74-2
• Molecular Weight: 402.288
• Mol File: 106729-74-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-cis-2,3-trans-2-benzamido-3-bromocyclohexyl benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-cis-2,3-trans-2-benzamido-3-bromocyclohexyl benzoate(106729-74-2)
• EPA Substance Registry System: 1,2-cis-2,3-trans-2-benzamido-3-bromocyclohexyl benzoate(106729-74-2)

Safety Data

• Hazardous Substances Data: 106729-74-2(Hazardous Substances Data)

Upstream product

• 614-28-8 dibenzoylimide 
• 614-28-8 N-benzoylbenzamide 
• 3413-44-3 (R)-2-cyclohexen-1-ol 
• 116429-76-6 ((3aS,4S,7aS)-4-Bromo-2-ethoxy-2-phenyl-hexahydro-benzooxazol-3-yl)-phenyl-methanone 
• 106729-73-1 cyclohex-2-enyl-N-benzoylbenzimidate 

Downstream Products

• 57707-58-1 cis-2-benzamidocyclohexyl benzoate 
• 106729-75-3 1,2-cis-2,3-cis-2-aminocyclohexane-1,3-diyl dibenzoate hydrochloride 
• 5450-83-9 N-(cis-2-hydroxycyclohexyl)benzamide 
• 5456-63-3 trans-2-hydroxycyclohexylamine hydrochloride 
• 156957-54-9 2-aminocyclohexane-1,3-diol 
• 3215-07-4 1,2-cis-2,3-cis-2-acetamidocyclohexane-1,3-diyl diacetate 
• 106729-76-4 1,2-cis-2,3-cis-2-(o-hydroxybenzylideneamino)cyclohexane-1,3-diyl dibenzoate 
• 106729-76-4 C₂₇H₂₅NO₅ 

Relevant articles and documents

Stereocontrolled Preparation of Cyclohexane Amino Alcohols Utilising a Modified Mitsunobu Reaction

A method for the introduction of amino groups into aliphatic systems is described.Cyclohex-2-enol reacts with aromatic diacylamines under Mitsunobu reaction conditions to give either N-alkylated or O-alkylated products in a controlled, predictable manner.

NEW ROUTES TO CIS-1,2-HYDROXYAMINES AND RELATED SYSTEMS

Use of modified Mitsunobu reactions followed by intramolecular cyclisations have been used to prepare cis-1,2-hydroxyamines, cis-1,3-hydroxyamines, 1,2,3-dihydroxyamines and 1,2,3-diaminoalcohols from allylic alcohols