CAS 118291-90-0

2-chloro-4-nitrophenylmaltotrioside

Description:

2-Chloro-4-nitrophenylmaltotrioside is a synthetic compound that belongs to the class of glycosides, specifically a maltotrioside derivative. It features a maltotrioside moiety, which is a carbohydrate composed of three glucose units linked together, and is modified by the presence of a 2-chloro-4-nitrophenyl group. This substitution introduces both a chlorine atom and a nitro group, which can influence the compound's reactivity and solubility. The presence of the nitro group typically enhances the compound's electrophilicity, making it useful in various chemical reactions, including those involving nucleophiles. This compound is often utilized in biochemical research, particularly in studies related to enzyme activity, as it can serve as a substrate for glycoside hydrolases. Its unique structural features may also impart specific biological activities, making it of interest in pharmacological studies. As with many synthetic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.

Formula: C₂₄H₃₄ClNO₁₈

InChI: InChI=1/C24H34ClNO18/c25-9-3-7(26(38)39)1-2-8(9)24(44-23-20(37)17(34)14(31)11(5-28)41-23)21(18(35)15(32)12(6-29)43-24)42-22-19(36)16(33)13(30)10(4-27)40-22/h1-3,10-23,27-37H,4-6H2/t10-,11-,12-,13-,14-,15-,16+,17+,18+,19-,20-,21-,22-,23-,24-/m1/s1

InChI key: AQTOSAZILYIEIC-LTCRKWBUSA-N

SMILES: C1=CC(=C(C=C1[N+](=O)[O-])Cl)[C@]2([C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O[C@@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O

Synonyms:

• 2-Chloro-4-nitrophenyl-α-D-maltotrioside

2-Chloro-4-nitrophenyl α-D-maltotrioside

CAS: 118291-90-0

Formula: C₂₄H₃₄ClNO₁₈

Purity: 99%

Color and Shape: Solid

Molecular weight: 659.9757

Ref: IN-DA01DQ0H

2-Chloro-4-nitrophenyl a-D-maltotrioside

CAS: 118291-90-0

Formula: C₂₄H₃₄ClNO₁₈

Purity: (HPLC) ≥ 95.0%

Color and Shape: Off-white to pale yellow powder

Molecular weight: 659.98

Ref: 7W-GC2222

G3-CNP

CAS: 118291-90-0

G3-CNP is a substrate for α-amylase and the hydrolysis product is 2-chloro-4-nitrophenol, enzyme activity by colorimetric assay at 405 nm.

Formula: C₂₄H₃₄ClNO₁₈

Purity: 98.53%

Color and Shape: White Solid

Molecular weight: 659.98

Ref: TM-T37834

2-Chloro-4-nitrophenyl a-D-Maltotrioside

CAS: 118291-90-0

Formula: C₂₄H₃₄ClNO₁₈

Color and Shape: Neat

Molecular weight: 659.98

Ref: TR-C596473

G3-CNP

CAS: 118291-90-0

(2R,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6R)-6-(((2R,3S,4R,5R,6R)-6-(2-Chloro-4-nitrophenoxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-tri

Formula: C₂₄H₃₄ClNO₁₈

Purity: 99%

Molecular weight: 659.98

Ref: IN-DG294262

2-Chloro-4-nitrophenyl α-D-maltotrioside

CAS: 118291-90-0

2-Chloro-4-nitrophenyl α-D-maltotrioside

Formula: C₂₄H₃₄ClNO₁₈

Purity: 99%

Color and Shape: Solid-Crystals

Molecular weight: 659.97566

Ref: 54-BITJ0002

2-Chloro-4-nitrophenyl a-D-maltotrioside

CAS: 118291-90-0

2-Chloro-4-nitrophenyl a-D-maltotrioside (2CNP) is a potent hypoglycemic agent that has been shown to decrease postprandial blood glucose levels in humans. 2CNP is a white crystalline solid that is soluble in water and ethanol. The transfer reactions of 2CNP are enhanced by benzalkonium chloride, which forms an organic complex with the drug. The optimum concentration for the hypoglycemic effect of 2CNP is determined to be 10 μM, which can be detected using an optical sensor. This compound also inhibits α-amylase and other enzymes involved in carbohydrate metabolism, leading to the accumulation of glycogen and lowering the blood glucose level.

Formula: C₂₄H₃₄CiNO₁₈

Purity: Min. 95%

Color and Shape: Off-White Yellow Powder

Molecular weight: 659.98 g/mol

Ref: 3D-EC09787

2-Chloro-4-Nitrophenyl a-D-Maltotrioside (CNPG3) extrapure, 95%

CAS: 118291-90-0

Formula: C₂₄H₃₄ClNO₁₈

Purity: min. 95%

Color and Shape: Pale yellow, Crystalline compound

Molecular weight: 659.98

Ref: SR-48958