92265-07-1

Basic information

• Product Name: Benzamide, N-[1-(hydroxymethyl)-2-methylpropyl]-
• CAS NO: 92265-07-1
• Molecular Formula: C12H17NO2
• Molecular Weight: 207.26900
• Mol File: 92265-07-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzamide, N-[1-(hydroxymethyl)-2-methylpropyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-[1-(hydroxymethyl)-2-methylpropyl]-(92265-07-1)
• EPA Substance Registry System: Benzamide, N-[1-(hydroxymethyl)-2-methylpropyl]-(92265-07-1)

Safety Data

• Hazardous Substances Data: 92265-07-1(Hazardous Substances Data)

Upstream product

• 4380-77-2 O-phenylbenzohydroxamic acid 
• 98-88-4 benzoyl chloride 
• 227080-13-9 2-(4-bromo-phenyl)-4-isopropyl-4,5-dihydro-oxazole 
• 4491-47-8 2-phenyl-4-isopropylidene-5(4H)oxazolone 
• 16369-05-4 valinol 

Downstream Products

• 1218937-28-0 C₁₂H₁₅NS 
• 479672-27-0 N-(1-formyl-2-methylpropyl)benzamide 
• 1492-13-3 (2R)-2-(benzoylamino)-3-methylbutyric acid methyl ester 
• 1492-13-3 N-benzoyl-L-valine methyl ester 
• 916685-60-4 (S)-2-benzamido-3-methylbutyl benzoate 

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.

A Convenient Synthesis of α-Acylamino Alcohols from Azlactones

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