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4-(4-Dimethylaminophenylazo) beta-lactoside, also known as beta-lactoside, is a glycoside derived from beta-lactose with a p-(p-dimethylaminophenylazo)phenyl group attached at the 1-position. 4-(4-Dimethylaminophenylazo) beta-lactoside is characterized by its unique chemical structure and potential applications in various fields.

27597-77-9

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27597-77-9 Usage

Uses

Used in Chemical Synthesis:
4-(4-Dimethylaminophenylazo) beta-lactoside is used as an intermediate in the synthesis of various organic compounds, particularly those involving the formation of complex glycosidic linkages. Its unique structure allows for the creation of novel molecules with potential applications in pharmaceuticals, agrochemicals, and other industries.
Used in Analytical Chemistry:
In analytical chemistry, 4-(4-Dimethylaminophenylazo) beta-lactoside serves as a valuable reagent for the detection and quantification of specific analytes. Its distinctive chromophore enables the development of colorimetric or fluorometric assays, which can be employed for the sensitive and selective determination of target molecules in complex samples.
Used in Pharmaceutical Research:
4-(4-Dimethylaminophenylazo) beta-lactoside is utilized as a key building block in the design and development of new pharmaceutical agents. Its unique structure can be exploited to create novel drug candidates with improved pharmacological properties, such as enhanced solubility, bioavailability, and target selectivity.
Used in Material Science:
In the field of material science, 4-(4-Dimethylaminophenylazo) beta-lactoside can be employed as a functional component in the development of advanced materials with specific properties. For instance, its incorporation into polymer matrices can lead to materials with tailored optical, electronic, or mechanical characteristics, depending on the desired application.
Used in Biomedical Research:
4-(4-Dimethylaminophenylazo) beta-lactoside also holds potential in biomedical research, where it can be used to study the interactions between carbohydrates and proteins, such as lectins. This knowledge can be applied to develop new strategies for the detection, prevention, or treatment of various diseases, including cancer and infectious diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 27597-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,5,9 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27597-77:
(7*2)+(6*7)+(5*5)+(4*9)+(3*7)+(2*7)+(1*7)=159
159 % 10 = 9
So 27597-77-9 is a valid CAS Registry Number.
InChI:InChI=1/C26H35N3O11/c1-29(2)15-7-3-13(4-8-15)27-28-14-5-9-16(10-6-14)37-25-23(36)21(34)24(18(12-31)39-25)40-26-22(35)20(33)19(32)17(11-30)38-26/h3-10,17-26,30-36H,11-12H2,1-2H3/b28-27+/t17-,18-,19+,20+,21-,22-,23-,24-,25-,26+/m1/s1

27597-77-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-{[4-(dimethylamino)phenyl]diazenyl}phenyl-β-lactoside

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:27597-77-9 SDS

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