70935-14-7

Basic information

• Product Name: 3-Hydroxyphenylglyoxal
• Synonyms: 2-(3-hydroxyphenyl)-2-oxoacetaldehyde;3-hydroxyphenylglyoxal;70935-14-7;(3-Hydroxyphenyl)glyoxal;SCHEMBL3539849;BFHONQWJUMCAKI-UHFFFAOYSA-N;EN300-190266;Z1255357387
• CAS NO: 70935-14-7
• Molecular Formula: C8H6O3
• Molecular Weight: 150.134
• Mol File: 70935-14-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-Hydroxyphenylglyoxal(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Hydroxyphenylglyoxal(70935-14-7)
• EPA Substance Registry System: 3-Hydroxyphenylglyoxal(70935-14-7)

Safety Data

• Hazardous Substances Data: 70935-14-7(Hazardous Substances Data)

Upstream product

• 121-71-1 3-Hydroxyacetophenone 
• 7446-08-4 selenium(IV) oxide 
• 100-83-4 meta-hydroxybenzaldehyde 

Downstream Products

• 103656-55-9 3'-Hydroxyphenyl-isonitrosomethylketon 
• 925705-73-3 TG₁₀₀₁₁₀ 
• 70935-18-1 7-Amino-4-(3-hydroxy-phenyl)-1-methyl-1H-pyrimido[4,5-c]pyridazin-5-one 
• 80082-15-1 7-Amino-3-(3-hydroxy-phenyl)-1-methyl-1H-pyrimido[4,5-c]pyridazin-5-one 
• 52093-42-2 Neosynephrine ketone 
• 872812-24-3 2-(3-hydroxyphenyl)quinoxaline 
• 22510-12-9 2-ethylamino-1-(3-hydroxy-phenyl)-ethanone 

Relevant articles and documents

Synthesis of α-keto aldehydes via selective Cu(i)-catalyzed oxidation of α-hydroxy ketones

An efficient approach to synthesize α-keto aldehydes was established through selective oxidation of α-hydroxy ketones catalyzed by Cu(i) using oxygen as oxidant. A wide array of α-keto aldehydes was prepared with isolated yields of up to 87%. The potential utilization of this reaction was evaluated by gram-scale reactions and synthetic applications.

Kinetics and mechanism of oxidation of o-, m- and p-hydroxy-acetophenones by hexacyanoferrate(III) in alkaline medium

Oxidation of o-, p- and m-hydroxyacetophenones by hexacyanoferrate(III) in alkaline medium is first order each in and .Added KCl and increase in increase the rate.Activation parameters have been calculated and