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4-Azido-4-nitro-2,1,3-benzoxadiazole

Product Code:
 
CDX-A0177
Product Group:
 
Dyes, Stains, and Probes
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
+4°C
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Chemical Structure
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Chemical Structure

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CDX-A0177-M100100 mg£89.00
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CDX-A0177-M500500 mg£316.00
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This product comes from: Switzerland.
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Further Information

Alternate Names/Synonyms:
4-Azido-7-nitrobenzofurazan; 4-Azido-7-nitro-2,1,3-benzoxadiazole
Appearance:
Yellow crystalline powder.
CAS:
10199-90-3
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Keep cool and dry.Protect from light and moisture.
InChi:
InChI=1S/C6H2N6O3/c7-11-8-3-1-2-4(12(13)14)6-5(3)9-15-10-6/h1-2H
InChiKey:
YPRIQOMTFNRORM-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 10199-90-3. Formula: C6H2N6O3. MW: 206.12. Synthetic. Non-fluorescent azido fluorogen which can be photoactivated to the longer wavelength amino version that is fluorescent. Building block and reagent for synthesis of fluorescent probes. Used for the preparation of fluorogenic substrates, chemosensors and probes, which can be concerted to the high fluoresence NBD-amine after release. Fluorescent chemosensor for hydrogen sulfide. Spectral data: Ex=384 (454)nm, Em=550nm.
MDL:
MFCD23938487
Molecular Formula:
C6H2N6O3
Molecular Weight:
206.12
Package Type:
Vial
Product Description:
Non-fluorescent azido fluorogen which can be photoactivated to the longer wavelength amino version that is fluorescent. Building block and reagent for synthesis of fluorescent probes. Used for the preparation of fluorogenic substrates, chemosensors and probes, which can be concerted to the high fluoresence NBD-amine after release. Fluorescent chemosensor for hydrogen sulfide. Spectral data: Ex=384 (454)nm, Em=550nm.
Purity:
>99% (HPLC)
SMILES:
[O-][N+](=O)C1=CC=C(N=[N+]=[N-])C2=NON=C12
Solubility Chemicals:
Soluble in chloroform.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Fluorescent Reagents
UNSPSC Number:
41105331
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

References

(1) S.J. Lord, et al.; J. Phys. Chem. B 114, 14157 (2010) | (2) J.A. Key & C.W. Cairo; Dyes Pigments 88, 95 (2011) | (3) A. Brown, et al.; J. Phys. Chem. A 116, 46 (2012) | (4) G. Zhou, et al.; Tetrahedron 69, 867 (2013)