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2295-58-1,MFCD00016456
Catalog No.:AA002LKR

2295-58-1 | 2',4',6'-Trihydroxypropiophenone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
95%
in stock  
$6.00   $4.00
- +
25mg
95%
in stock  
$9.00   $7.00
- +
100mg
95%
in stock  
$16.00   $11.00
- +
250mg
95%
in stock  
$25.00   $18.00
- +
1g
99%
in stock  
$50.00   $35.00
- +
5g
99%
in stock  
$100.00   $70.00
- +
25g
>98.0%(GC)(T)
in stock  
$134.00   $94.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA002LKR
Chemical Name:
2',4',6'-Trihydroxypropiophenone
CAS Number:
2295-58-1
Molecular Formula:
C9H10O4
Molecular Weight:
182.1733
MDL Number:
MFCD00016456
SMILES:
CCC(=O)c1c(O)cc(cc1O)O
Properties
Properties
 
BP:
341.7°C at 760 mmHg  
Form:
Solid  
MP:
177°C  
Refractive Index:
1.4500 (estimate)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
180  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
2  
XLogP3:
1.6  

Upstream Synthesis Route

[1]AgriculturalandBiologicalChemistry,1985,vol.49,#3,p.719-724

[2]EuropeanJournalofMedicinalChemistry,2014,vol.85,p.621-628

[3]AustralianJournalofChemistry,2005,vol.58,#7,p.551-555

[4]EuropeanJournalofMedicinalChemistry,2018,vol.155,p.255-262

[5]BioorganicandMedicinalChemistry,2006,vol.14,#13,p.4402-4409

[6]PhytochemistryLetters,2012,vol.5,#1,p.144-149

[7]Molecules,2014,vol.19,#8,p.11645-11659

[8]Bioscience,Biotechnology,andBiochemistry,1992,vol.56,#12,p.2062-2063

[9]AustralianJournalofChemistry,2008,vol.61,#9,p.718-724

[10]EuropeanJournalofMedicinalChemistry,2017,vol.125,p.492-499

[11]Molecules,2018,vol.23,#10,

[12]MedChemComm,2018,vol.9,#10,p.1698-1707

[1]OrganicLetters,2004,vol.6,#25,p.4647-4650

[2]Patent:EP2660240,2013,A1,

[3]Patent:US2013/303544,2013,A1,

[1]JournaloftheChemicalSociety,1931,p.1255,1264

[2]JournaloftheAmericanChemicalSociety,1932,vol.54,p.2452

[3]JournaloftheSouthAfricanChemicalInstitute,1943,vol.26,p.41,45

[4]YakugakuZasshi,1949,vol.69,p.431

[5]Chem.Abstr.,1950,p.3457

[6]Phytochemistry(Elsevier),1983,vol.22,#1,p.243-246

[1]Tetrahedron,1969,vol.25,p.707-714

[1]JournaloftheSouthAfricanChemicalInstitute,1943,vol.26,p.41,45

[2]JournalofHeterocyclicChemistry,2002,vol.39,#6,p.1251-1258

Downstream Synthesis Route
110-78-1    2295-58-1   
2,4,6-Trihydroxy-3-propionyl-N-propyl-benzamide 

[1]AgriculturalandBiologicalChemistry,1989,vol.53,p.1953-1960

[1]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1986,vol.25,p.478-480

542-85-8    2295-58-1   
N-Ethyl-2,4,6-trihydroxy-3-propionyl-thiobenzamide 

[1]AgriculturalandBiologicalChemistry,1987,vol.51,p.2607-2608

628-30-8    2295-58-1   
2,4,6-Trihydroxy-3-propionyl-N-propyl-thiobenzamide 

[1]AgriculturalandBiologicalChemistry,1987,vol.51,p.2607-2608

3954-13-0    2295-58-1   
2,4,6-Trihydroxy-N-pentyl-3-propionyl-benzamide 

[1]AgriculturalandBiologicalChemistry,1989,vol.53,p.1953-1960

Literature

Title: Self-assembled light-harvesting peptide nanotubes for mimicking natural photosynthesis.

Journal: Angewandte Chemie (International ed. in English) 20120109

Title: Facilitation of expulsion of ureteral stones by addition of α1-blockers to conservative therapy.

Journal: Scandinavian journal of urology and nephrology 20101201

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: Positively charged calcium phosphate/polymer nanoparticles for photodynamic therapy.

Journal: Journal of materials science. Materials in medicine 20100301

Title: Different measures of molecular mobility: comparison between calorimetric and thermally stimulated current relaxation times below Tg and correlation with dielectric relaxation times above Tg.

Journal: Journal of pharmaceutical sciences 20081001

Title: Prediction of onset of crystallization from experimental relaxation times. II. Comparison between predicted and experimental onset times.

Journal: Journal of pharmaceutical sciences 20080101

Title: Predictions of onset of crystallization from experimental relaxation times I-correlation of molecular mobility from temperatures above the glass transition to temperatures below the glass transition.

Journal: Pharmaceutical research 20061001

Title: Burns SM, et al. High-throughput luminescent reporter of insulin secretion for discovering regulators of pancreatic Beta-cell function. Cell Metab. 2015 Jan 6;21(1):126-37.

Title: C Barlow, et al. Modulation of neurogenesis using d-cycloserine combinations. 2010-08-26. PAT - US2010216805.

Title: Ohgaki K, et al. Facilitation of expulsion of ureteral stones by addition of α1-blockers to conservative therapy. Scand J Urol Nephrol. 2010 Dec;44(6):420-4.

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Tags:2295-58-1 Molecular Formula|2295-58-1 MDL|2295-58-1 SMILES|2295-58-1 2',4',6'-Trihydroxypropiophenone