2,8-Dibenzyl-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one | CAS No. 70217-82-2

2,8-Dibenzyl-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one

Basic Information

CAS Number

70217-82-2

Molecular Formula

C26H21N3O

Molecular Weight

391.47 g/mol

AD

Basic Physical Properties

Density

1.20±0.1 g/cm3 (20 ºC 760 Torr),

Solubility

Insuluble (2.2E-3 g/L) (25 ºC),

C1=CC=C(C=C1)CC2=C(N3C=C(N=C(C3=N2)CC4=CC=CC=C4)C5=CC=CC=C5)O

InChI

InChI=1S/C26H21N3O/c30-26-23(17-20-12-6-2-7-13-20)28-25-22(16-19-10-4-1-5-11-19)27-24(18-29(25)26)21-14-8-3-9-15-21/h1-15,18,27H,16-17H2

InChIKey

MWOYPGFRXPPBOX-UHFFFAOYSA-N

LogP

4.847000000000004

Topological Polar Surface Area

50.68 Ų

Hydrogen Bond Donor/Acceptor

1 / 4

Complexity

524

Synonyms & References

English

  • AKOS030213259
  • Coelenterazine 400 a is known as a bisdeoxy derivative of coelenterazine.
  • HY-118462
  • C-7011
  • 2,8-dibenzyl-6-phenylimidazo[1,2-a]pyrazin-3-ol
  • DTXSID10628592
  • FT-0698871
  • 2,8-dibenzyl-6-phenyl-7H-imidazo[1,2-a]pyrazin-3-one
  • TQP1618
  • C-7010
  • 2,8-dibenzyl-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one
  • 70217-82-2
  • SCHEMBL492636
  • Coelenterazine 400 a
  • MWOYPGFRXPPBOX-UHFFFAOYSA-N
  • Coelenteramine 400a
  • BlueSyn C
  • MFCD04114093
  • Coelenterazine 400a
  • coelenterazine-400a
  • CS-0066034
  • coelenterazine 400 a
  • BISDEOXYCOELENTERAZINE
  • coelenterazine-hh
  • DI-DEHYDRO COELENTERAZINE
  • 6-Phenyl-2,8-bis(phenylmethyl)imidazo[1,2-a]pyrazin-3(7H)-one
  • Coelenterazine HH
  • DeepBlueC

MDL Number

MFCD04114093

FAQ

What regulatory guidelines apply to 2,8-Dibenzyl-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one (CAS: 70217-82-2)?

2,8-Dibenzyl-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one is subject to various regulatory guidelines including GHS classification for its hazardous properties, REACH regulations for its registration, evaluation, and authorization in the European Union, and FDA/EPA requirements for its use in pharmaceuticals and environmental applications.

Are there alternatives to 2,8-Dibenzyl-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one in its synthesis?

Alternative reagents for synthesizing 2,8-Dibenzyl-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one include various benzyl compounds and imidazopyrazine precursors. Isomers and analogs such as 2,8-diaryl-6-phenylimidazo[1,2-a]pyrazines can also be used as substitutes.

What is the market or research trend for 2,8-Dibenzyl-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one?

The market for 2,8-Dibenzyl-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one is expanding in pharmaceuticals and research due to its anti-inflammatory and anti-cancer properties. Research trends include exploring its use in targeted drug delivery systems and as a lead compound in drug discovery.

How should waste containing 2,8-Dibenzyl-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one be handled?

Waste containing 2,8-Dibenzyl-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one should be collected in sealed containers and stored in a cool, well-ventilated area away from sources of ignition. For disposal, professional waste management services should be employed to ensure safe incineration or other environmentally friendly methods are used.

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