4-Nitrophenyl α-D-mannopyranoside

Names

[ Name ]:
4-Nitrophenyl α-D-mannopyranoside

[Synonym ]:
MFCD00066002
p-nitrophenyl mannoside
4-Nitrophenyl α-D-mannopyranoside
4-NITROPHENYL-A-D-MANNOSIDE
EINECS 233-776-6
MAN1-A-PNP
α-D-Mannopyranoside, 4-nitrophenyl
p-Nitrophenyl Alpha-D-Mannopyranoside
4-Nitrophenyl α-D-Mannopyranoside [Substrate
4-Nitrophenyla-D-mannopyranoside
4-Nitrophenyl-alpha-D-Mannopyranoside

Biological Activity

[Description]:

p-Nitrophenyl α-D-mannopyranoside is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
582.2±50.0 °C at 760 mmHg

[ Melting Point ]:
179-181ºC

[ Molecular Formula ]:
C₁₂H₁₅NO₈

[ Molecular Weight ]:
301.249

[ Flash Point ]:
305.9±30.1 °C

[ Exact Mass ]:
301.079773

[ PSA ]:
145.20000

[ LogP ]:
-0.55

[ Vapour Pressure ]:
0.0±1.7 mmHg at 25°C

[ Index of Refraction ]:
1.648

[ Storage condition ]:
2-8°C

[ Water Solubility ]:
DMF: 50 mg/mL, clear, very faintly yellow

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
24/25-36-26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2932999099

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2932999099

[ Summary ]:
2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Synthesis of glycopeptide dendrimers, dimerization and affinity for Concanavalin A.

Bioorg. Med. Chem. 19 , 2879-87, (2011)

We described herein the synthesis of second generation glycopeptide dendrimers G2a-g presenting variable amino acids placed internally into the multivalent scaffold. The effect of such structural modu...

ABC transporter A3 facilitates lysosomal sequestration of imatinib and modulates susceptibility of chronic myeloid leukemia cell lines to this drug.

Haematologica 94 , 1528-36, (2009)

Inhibition of BCR-ABL tyrosine kinase activity has evolved as a mainstay of therapy for patients with chronic myeloid leukemia. However, a fraction of leukemic cells persists under targeted therapy an...

Mechanistic insights into a Ca2+-dependent family of alpha-mannosidases in a human gut symbiont.

Nat. Chem. Biol. 6 , 125-32, (2010)

Colonic bacteria, exemplified by Bacteroides thetaiotaomicron, play a key role in maintaining human health by harnessing large families of glycoside hydrolases (GHs) to exploit dietary polysaccharides...