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Chemical Structure| 1075-06-5 Chemical Structure| 1075-06-5
Chemical Structure| 1075-06-5

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Phenylglyoxal Hydrate is a potent inhibitor of mitochondrial aldehyde dehydrogenase (ALDH), binding the arginine residues in purified Hageman factor (HF, Factor XII) and causes inhibition of its coagulant properties.

Synonyms: Phenylglyoxal hydrate; 1-Phenylethanedione hydrate

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Product Details of 2,2-Dihydroxy-1-phenylethan-1-one

CAS No. :1075-06-5
Formula : C8H8O3
M.W : 152.15
SMILES Code : OC(O)C(C1=CC=CC=C1)=O
Synonyms :
Phenylglyoxal hydrate; 1-Phenylethanedione hydrate
MDL No. :MFCD00149499
InChI Key :NBIBDIKAOBCFJN-UHFFFAOYSA-N
Pubchem ID :99611

Safety of 2,2-Dihydroxy-1-phenylethan-1-one

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 2,2-Dihydroxy-1-phenylethan-1-one

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1075-06-5 ]

[ 1075-06-5 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 54030-56-7 ]
  • [ 1075-06-5 ]
  • [ 126-81-8 ]
  • 5-(2-hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-3-methyl-2-(methylsulfanyl)-6-phenyl-7H-pyrrolo[2,3-d]pyrimidin-4(3H)-one [ No CAS ]
  • 2
  • [ 1075-06-5 ]
  • [ 123639-56-5 ]
  • methyl (3R,5S)-4-benzyl-6-oxo-5-phenyl-morpholine-3-carboxylate [ No CAS ]
  • methyl (3R,5R)-4-benzyl-6-oxo-5-phenyl-morpholine-3-carboxylate [ No CAS ]
  • 3
  • [ 57772-50-6 ]
  • [ 1075-06-5 ]
  • [ 333-20-0 ]
  • 9-methyl-3-phenyl-5H-benzo[d]imidazo[5,1-b][1,3]oxazine-1(2H)-thione [ No CAS ]
  • 4
  • [ 504-29-0 ]
  • [ 52851-41-9 ]
  • [ 1075-06-5 ]
  • 4-hydroxy-3-(2-phenylimidazo[1,2-a]pyridin-3-yl)quinolin-2(1H)-one [ No CAS ]
  • 5
  • [ 1075-06-5 ]
  • [ 5552-83-0 ]
  • [ 251940-06-4 ]
  • (4-fluorophenyl)(6-((6-methylpyridin-2-yl)methyl)-5-phenyl-2,3-dihydro-1H-pyrrolo[1,2-a]imidazol-7-yl)methanone [ No CAS ]
  • 6
  • [ 1075-06-5 ]
  • [ 82100-22-9 ]
  • [ 5552-83-0 ]
  • (4-bromophenyl)(6-((6-methylpyridin-2-yl)methyl)-5-phenyl-2,3-dihydro-1H-pyrrolo[1,2-a]imidazol-7-yl)methanone [ No CAS ]
  • 7
  • [ 4139-61-1 ]
  • [ 1075-06-5 ]
  • [ 115859-76-2 ]
  • (E)-6-bromo-3-(6-hydroxy-8-(4-methylbenzoyl)-6-phenyl-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrimidin-7(6H)-ylidene)chromane-2,4-dione [ No CAS ]
YieldReaction ConditionsOperation in experiment
87% In 1,4-dioxane; at 100℃; for 10h; Add 10 mL of 1,4-dioxane as a solvent to a 25 mL round bottom flask. Then add benzoyl formaldehyde hydrate, 4-hydroxycoumarin, and 2- (tetrahydropyrimidine-2 (1H) -subunit) -1- (p-tolyl) ethyl-1-one, Where the molar ratio of benzoyl formaldehyde hydrate, <strong>[4139-61-1]6-bromo-4-hydroxycoumarin</strong> and 2- (tetrahydropyrimidine-2 (1H) -subunit) -1- (p-tolyl) ethyl-1-one Is 1: 1: 1, The ratio of the molar amount of the benzoyl formaldehyde derivative (benzoyl formaldehyde hydrate) to the volume of the solvent mol: L is 1:10; Stir the reaction at a temperature of 100 C. Use TLC to detect the reaction to 10h, The reaction liquid was completely obtained from the reaction of the raw materials. The reaction liquid was cooled to room temperature, and purified by column chromatography to obtain a chromone-substituted 2-hydroxypyrrole derivative ((E) -6-bromo-3- (6-hydroxy- 8- (4-methylbenzoyl) -6-phenyl-1,2,3,4-tetrahydropyrrolo [1,2-a] pyrimidine-7 (6H) -subunit) chroman-2 , 4-dione); wherein the column chromatography eluent is a mixed solvent of ethyl acetate / petroleum ether, and the volume ratio of ethyl acetate to petroleum ether is 2: 1;
  • 8
  • [ 4139-61-1 ]
  • [ 1075-06-5 ]
  • 2-nitro-N-(p-tolyl)ethene-1,1-diamine [ No CAS ]
  • 6-bromo-4-hydroxy-3-(4-nitro-2-phenyl-5-(p-tolylamino)-1Hpyrrol-3-yl)-2H-chromen-2-one [ No CAS ]
 

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