5450-83-9

Basic information

• Product Name: N-(2-hydroxycyclohexyl)benzamide
• CAS NO: 5450-83-9
• Molecular Formula: C₁₃H₁₇NO₂
• Molecular Weight: 219.2796
• Mol File: 5450-83-9.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 445.4°C at 760 mmHg
• Flash Point: 223.1°C
• Density: 1.15g/cm³
• Vapor Pressure: 1.03E-08mmHg at 25°C
• Refractive Index: 1.57
• CAS DataBase Reference: N-(2-hydroxycyclohexyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-hydroxycyclohexyl)benzamide(5450-83-9)
• EPA Substance Registry System: N-(2-hydroxycyclohexyl)benzamide(5450-83-9)

Safety Data

• Hazardous Substances Data: 5450-83-9(Hazardous Substances Data)

Upstream product

• 614-80-2 2-(acetylamino)phenol 
• 123132-86-5 cis-2-benzamidocyclohexyl acetate 
• 106729-74-2 1,2-cis-2,3-trans-2-benzamido-3-bromocyclohexyl benzoate 
• 106729-73-1 cyclohex-2-enyl-N-benzoylbenzimidate 
• 4380-77-2 O-phenylbenzohydroxamic acid 
• 57437-13-5 2-phenyl-3a,4,5,6,7,7a-hexahydrobenzo[d]oxazole 
• 57707-58-1 (+/-)-trans-1-benzoylamino-2-benzoyloxy-cyclohexane 
• 123132-86-5 (+/-)-trans-1-acetoxy-2-benzoylamino-cyclohexane 
• 4050-48-0 trans-2-nitro-cyclohexanol 
• 98-88-4 benzoyl chloride 
• 931-16-8 (+/-)-trans-2-aminocyclohexanol 
• 6850-38-0 2-aminocyclohexanol 
• 118311-85-6 (1S,6S)-6-Nitro-cyclohex-3-enol 
• 123132-85-4 1,2-cis-2,3-trans-2-benzamido-3-bromocyclohexyl acetate 

Downstream Products

• 3721-20-8 N-(2-chlorocyclohexyl)benzamide 
• 100609-14-1 (+/-)-benzoic acid-(cis-2-amino-cyclohexyl ester) 
• 38898-70-3 cis-2-amino-cyclohexanol-⁽¹⁾ 
• 5450-83-9 N-(cis-2-hydroxycyclohexyl)benzamide 
• 100609-14-1 (+/-)-benzoic acid-(trans-2-amino-cyclohexyl ester) 
• 57437-13-5 (3aR,7aS)-2-phenyl-3a,4,5,6,7,7a-hexahydrobenzo[d]oxazole 
• 5456-63-3 trans-2-hydroxycyclohexylamine hydrochloride 
• 137858-58-3 2-benzamidocyclohexanone 
• 57707-58-1 cis-2-benzamidocyclohexyl benzoate 
• 110149-86-5 (+/-)-cis-1-benzoylamino-2-(toluene-4-sulfonyloxy)-cyclohexane 
• 141478-35-5 cis-2-benzamido-N-(1-phenylethyl)-cyclohexanamine 
• 141553-10-8 trans-2-benzamido-N-(1-phenylethyl)-cyclohexanamine 
• 141478-36-6 cis-2-benzamido-cyclohexanamine 
• 141478-36-6 N-((1S,2S)-2-aminocyclohexyl)benzamide 

Relevant articles and documents

Catalytic Alkene Difunctionalization via Imidate Radicals

The first catalytic strategy to harness imidate radicals has been developed. This approach enables alkene difunctionalization of allyl alcohols by photocatalytic reduction of their oxime imidates. The ensuing imidate radicals undergo consecutive intra- and intermolecular reactions to afford (i) hydroamination, (ii) aminoalkylation, or (iii) aminoarylation, via three distinct radical mechanisms. The broad scope and utility of this catalytic method for imidate radical reactivity is presented, along with comparisons to other N-centered radicals and complementary, closed-shell imidate pathways.

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