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N1377

Sigma-Aldrich

4-Nitrophenyl α-D-glucopyranoside

chromogenic, ≥99%, powder or crystals

Sinonimo/i:

p-Nitrophenyl α-D-glucopyranoside

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About This Item

Formula empirica (notazione di Hill):
C12H15NO8
Numero CAS:
3767-28-0
Peso molecolare:
301.25
Beilstein:
92212
Numero CE:
223-189-3
Numero MDL:
MFCD00064088
Codice UNSPSC:
12352204
ID PubChem:
24897484
NACRES:
NA.32

product name

4-Nitrophenyl α-D-glucopyranoside, ≥99%

Livello qualitativo

300

Saggio

≥99%

Forma fisica

powder or crystals

Solubilità

methanol: 20 mg/mL, clear to very slightly hazy, colorless to greenish-yellow

Temperatura di conservazione

−20°C

Stringa SMILE

OC[C@H]1O[C@H](Oc2ccc(cc2)[N+]([O-])=O)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C12H15NO8/c14-5-8-9(15)10(16)11(17)12(21-8)20-7-3-1-6(2-4-7)13(18)19/h1-4,8-12,14-17H,5H2/t8-,9-,10+,11-,12+/m1/s1
IFBHRQDFSNCLOZ-ZIQFBCGOSA-N

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Applicazioni

4-Nitrophenyl ǥ-D-glucopyranoside has been used as a substrate in an ǥ-glucosidase inhibition assay.

Azioni biochim/fisiol

4-Nitrophenyl ǥ-D-glucopyranoside serves as a substrate for glycosidases. Upon cleavage, the substrate is converted to a yellow-colored product.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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Herein, substituted imidazole-pyrazole hybrids (2a-2n) were prepared via a multi component reaction employing pyrazole-4-carbaldehydes (1a-1d), ammonium acetate, benzil and arylamines as reactants. All the new compounds were characterized through their spectral and elemental analyses. Further these compounds were tested against
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