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3476-89-9,MFCD00047564
Catalog No.:AA00BZDV

3476-89-9 | 1,2,3,4-Tetrahydro-quinoxaline

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$8.00   $6.00
- +
5g
97%
in stock  
$13.00   $9.00
- +
10g
97%
in stock  
$23.00   $16.00
- +
25g
97%
in stock  
$50.00   $35.00
- +
100g
97%
in stock  
$195.00   $137.00
- +
  • 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:
AA00BZDV
Chemical Name:
1,2,3,4-Tetrahydro-quinoxaline
CAS Number:
3476-89-9
Molecular Formula:
C8H10N2
Molecular Weight:
134.1784
MDL Number:
MFCD00047564
SMILES:
C1CNc2c(N1)cccc2
NSC Number:
48945
Properties
Properties
 
BP:
289.0°C  
Form:
Solid  
MP:
92-98 °C  
Refractive Index:
1.5579 (estimate)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
99.8  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Undefined Atom Stereocenter Count:
1  
XLogP3:
1.7  

Upstream Synthesis Route

[1]EuropeanJournalofOrganicChemistry,2012,#34,p.6752-6759

[1]Tetrahedron,2017,vol.73,#12,p.1618-1632

[1]Tetrahedron,2017,vol.73,#12,p.1618-1632

[2]Tetrahedron,2017,vol.73,#12,p.1618-1632

[3]Tetrahedron,2017,vol.73,#12,p.1618-1632

[4]Tetrahedron,2017,vol.73,#12,p.1618-1632

[1]Patent:WO2017/142883,2017,A1,.Locationinpatent:Paragraph0225;0227

[2]Patent:WO2016/86200,2016,A1,.Locationinpatent:Page/Pagecolumn230;231

[3]Patent:EP2172453,2010,A1,.Locationinpatent:Page/Pagecolumn17

Downstream Synthesis Route

[1]AdvancedSynthesisandCatalysis,2019,vol.361,p.2301-2308

[2]AustralianJournalofChemistry,1956,vol.9,p.397,402

[1]JournaloftheChemicalSociety,1952,p.4406,4408

[1]ChemistryofHeterocyclicCompounds,1983,vol.19,p.549-553    KhimiyaGeterotsiklicheskikhSoedinenii,1983,vol.19,p.677-681

[1]TetrahedronLetters,1988,vol.29,p.4115-4118

[1]JournalofOrganicChemistry,1992,vol.57,p.3303-3308

Literature

Title: Inter- and intramolecular Mitsunobu reaction and metal complexation study: synthesis of S-amino acids derived chiral 1,2,3,4-tetrahydroquinoxaline, benzo-annulated [9]-N3 peraza, [12]-N4 peraza-macrocycles.

Journal: Organic & biomolecular chemistry 20120227

Title: Organocatalytic sequential hetero-Diels-Alder and Friedel-Crafts reaction: constructions of fused heterocycles with scaffold diversity.

Journal: Organic letters 20111104

Title: rac-(2R,3S)-2-Phenyl-3-(3-phenyl-1,2,3,4-tetra-hydro-quinoxalin-2-yl)quinoxaline.

Journal: Acta crystallographica. Section E, Structure reports online 20080701

Title: 2,3-Bis(4-bromo-phen-yl)quinoxaline.

Journal: Acta crystallographica. Section E, Structure reports online 20080101

Title: Lewis acid-promoted annulation of O-quinonediimines by allylstannane: a facile synthesis of quinoxaline derivatives.

Journal: Organic letters 20041209

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Tags:3476-89-9 Molecular Formula|3476-89-9 MDL|3476-89-9 SMILES|3476-89-9 1,2,3,4-Tetrahydro-quinoxaline |Organic_Building_Blocks