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    Coumarine 314

    Available from stock

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      Coumarine 314

      SKU
      C0076

      Categories: Fluorescent Detection, Fluorescent Detection

      Synonyms
      C314, Coumarin 504, NSC 338967, 2,3,5,6-1H,4H-Tetrahydro-9-carbethoxyquinolizino-[9,9a,1-gh]coumarin
      55804-66-5
      CAS-Number
      C18H19NO4
      Molecular Formula
      313.35
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥98% (HPLC)
      Appearance
      Yellow to orange solid
      Identity
      1H-NMR

      Properties

      Solvents
      Soluble in ethanol or DMSO.
      Melting Point
      140-144 °C (lit.)
      UV / Vis
      λ ≤ 438 nm (EtOH) (lit.)
      Shipping
      AMBIENT
      Short Term Storage
      RT
      Long Term Storage
      RT
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at RT.
      Transportation
      Not dangerous goods
      Description
      Coumarin 314 is a rigidized aminocoumarin derivative used as a laser dye with an absorption maximum of 436nm. It can be used as starting material for the synthesis of fluorescent probes. Spectral data: λmax 436nm in ethanol, ε (extinction coefficient) ≥39000 at 389-401 nm in ethanol, λlaser 504nm.
      Smiles
      O=C1OC2=C3C4=C(CCCN4CCC3)C=C2C=C1C(OCC)=O
      InChi Key
      VMJKUPWQKZFFCX-UHFFFAOYSA-N
      References
      (1) G.A.Reynolds & K.H.Drexhage; Optics Commun. 13, 222 (1975) , (2) K.H.Drexhage; J. Res. Nati. Bureau Standards Sec. 1 - Phys. Chem. 80A, 421 (1976) , (3) A.N. Fletcher; Appl. Phys. 14, 295 (1977) , (4) A.J. Cox & B.K. Matise; Chem. Phys. Lett. 76, 125 (1980) , (5) A.N. Fletcher; Optics Commun. 48, 352 (1984) , (6) S. Speiser & N. Shakkour; Appl. Phys. B 38, 191 (1985) , (7) M.S.A. Abdel-Mottaleb; J. Photochem. Photobiol. A Chem. 50, 259 (1989) , (8) D.A. Pantano & D. Laria; J. Phys. Chem. B 107, 2971 (2003) , (9) A. Aspee, et al.; J. Phys. Chem. A 116, 199 (2012)
      InChi
      (1) F. Caturla et al.: Tetrahedron 60(8), 1903 (2004) , (2) I.K. Rhee et al.: Verpoorte, Phytochemical Analysis 14(3), 145 (2003) , (3) C.D. Voorhorst: Biochemical Pharmacology 20(6), 1321 (1971)

      Coumarin 314 is a rigidized aminocoumarin derivative used as a laser dye with an absorption maximum of 436nm. It can be used as starting material for the synthesis of fluorescent probes. Spectral data: λmax 436nm in ethanol, ε (extinction coefficient) ≥39000 at 389-401 nm in ethanol, λlaser 504nm.

      SKU: C0076 Categories: Fluorescent Detection, Fluorescent Detection
      • Additional information

      Additional information

      Synonyms

      C314, Coumarin 504, NSC 338967, 2,3,5,6-1H,4H-Tetrahydro-9-carbethoxyquinolizino-[9,9a,1-gh]coumarin

      Purity

      ≥98% (HPLC)

      Appearance

      Yellow to orange solid

      CAS-Number

      55804-66-5

      Molecular Formula

      C18H19NO4

      Molecular Weight

      313.35

      Identity

      1H-NMR

      Solvents

      Soluble in ethanol or DMSO.

      Melting Point

      140-144 °C (lit.)

      UV / Vis

      λ ≤ 438 nm (EtOH) (lit.)

      Smiles

      O=C1OC2=C3C4=C(CCCN4CCC3)C=C2C=C1C(OCC)=O

      InChi Key

      VMJKUPWQKZFFCX-UHFFFAOYSA-N

      Shipping

      AMBIENT

      Short Term Storage

      RT

      Long Term Storage

      RT

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at RT.

      Transportation

      Not dangerous goods

      References

      (1) G.A.Reynolds & K.H.Drexhage; Optics Commun. 13, 222 (1975), (2) K.H.Drexhage; J. Res. Nati. Bureau Standards Sec. 1 – Phys. Chem. 80A, 421 (1976), (3) A.N. Fletcher; Appl. Phys. 14, 295 (1977), (4) A.J. Cox & B.K. Matise; Chem. Phys. Lett. 76, 125 (1980), (5) A.N. Fletcher; Optics Commun. 48, 352 (1984), (6) S. Speiser & N. Shakkour; Appl. Phys. B 38, 191 (1985), (7) M.S.A. Abdel-Mottaleb; J. Photochem. Photobiol. A Chem. 50, 259 (1989), (8) D.A. Pantano & D. Laria; J. Phys. Chem. B 107, 2971 (2003), (9) A. Aspee, et al.; J. Phys. Chem. A 116, 199 (2012)

      InChi

      (1) F. Caturla et al.: Tetrahedron 60(8), 1903 (2004), (2) I.K. Rhee et al.: Verpoorte, Phytochemical Analysis 14(3), 145 (2003), (3) C.D. Voorhorst: Biochemical Pharmacology 20(6), 1321 (1971)

      Quantity

      500 mg, 1 g, Bulk

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