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Home Aldehydes 2065-75-0
2065-75-0,MFCD00459999
Catalog No.:AA00333T

2065-75-0 | 2-Bromomalonaldehyde

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
96%
in stock  
$7.00   $5.00
- +
25g
96%
in stock  
$13.00   $9.00
- +
50g
97%
in stock  
$20.00   $14.00
- +
  • 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:
AA00333T
Chemical Name:
2-Bromomalonaldehyde
CAS Number:
2065-75-0
Molecular Formula:
C3H3BrO2
Molecular Weight:
150.9587
MDL Number:
MFCD00459999
SMILES:
O=CC(C=O)Br
Properties
Properties
 
BP:
134.8°C at 760 mmHg  
Form:
Solid  
MP:
132-136 °C(lit.)  
Stability:
Air Sensitive  
Storage:
Inert atmosphere;-20 ℃;  

Computed Properties
 
Complexity:
53.8  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
2  
XLogP3:
0.2  

Upstream Synthesis Route

[1]Patent:US5089512,1992,A,

[1]Patent:WO2015/118019,2015,A1,.Locationinpatent:Page/Pagecolumn29

[2]JournalofMedicinalChemistry,2000,vol.43,#16,p.3168-3185

[3]YakugakuZasshi,1953,vol.73,p.276

[4]Chem.Abstr.,1954,p.2045

[1]Patent:WO2011/15343,2011,A1,.Locationinpatent:Page/Pagecolumn39-40

[2]Arkivoc,2016,vol.2016,#5,p.268-278

[1]MagneticResonanceinChemistry,2010,vol.48,#8,p.614-622

[1]Heterocycles,2015,vol.91,#5,p.1001-1006

Downstream Synthesis Route

[1]Patent:WO2015/118019,2015,A1.Locationinpatent:Page/Pagecolumn29

[2]JournalofMedicinalChemistry,2000,vol.43,p.3168-3185

[3]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1953,vol.73,p.276    Chem.Abstr.,1954,p.2045

[1]JournalofHeterocyclicChemistry,1991,vol.28,p.1747-1751

[2]JournalofMedicinalChemistry,1997,vol.40,p.470-478

[3]BioorganicandMedicinalChemistry,2003,vol.11,p.59-67

[4]JournalofMedicinalChemistry,2013,vol.56,p.4422-4441

[1]SyntheticCommunications,1988,vol.18,p.1187-1192

2065-75-0    2782-91-4   
S-(2-malonaldehyde)-1,1,3,3-tetramethylthiouroniumbromide 

[1]Wall,Mark;Benkovic,StephenJ.[JournalofHeterocyclicChemistry,2002,vol.39,#5,p.1097-1099]

[1]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.235-238

Literature

Title: 1-{4-Chloro-2-[2-(2-fluoro-phen-yl)-1,3-dithio-lan-2-yl]phen-yl}-2-methyl-1H-imidazole-5-carbaldehyde.

Journal: Acta crystallographica. Section E, Structure reports online 20110201

Title: 2-Chloro-6,6-dimethyl-5,6-dihydro-indazolo[2,3-c]quinazoline.

Journal: Acta crystallographica. Section E, Structure reports online 20100301

Title: Solid-phase synthesis of 4(5),1',5'-trisubstituted 2,4'-biimidazoles.

Journal: The Journal of organic chemistry 20091218

Title: Reaction routes leading to CO2 and CO in the Briggs-Rauscher oscillator: analogies between the oscillatory BR and BZ reactions.

Journal: The journal of physical chemistry. A 20090813

Title: Solid-phase synthesis of 7-substituted 3H-imidazo[2,1-i]purines.

Journal: Organic & biomolecular chemistry 20061221

Title: Reactions of 9-substituted guanines with bromomalondialdehyde in aqueous solution predominantly yield glyoxal-derived adducts.

Journal: Organic & biomolecular chemistry 20040707

Title: New nucleoside analogs from 2-amino-9-(beta-D-ribofuranosyl)purine.

Journal: Organic & biomolecular chemistry 20040321

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SDS
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