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2,3,4,5-tetra-O-acetyl-1-deoxy-1-(4,5-dimethyl-2-[(E)-(4-nitrophenyl)diazenyl]phenylamino)pentitol is a complex organic compound characterized by its pentitol backbone, to which five acetyl groups are attached. A distinctive feature of this molecule is the presence of a highly conjugated azobenzene moiety, which is linked to the pentitol. 2,3,4,5-tetra-O-acetyl-1-deoxy-1-(4,5-dimethyl-2-[(E)-(4-nitrophenyl)diazenyl]phenylamino)pentitol is known for its potential applications in various scientific fields due to its unique structural attributes.

6973-44-0

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6973-44-0 Usage

Uses

Used in Organic Synthesis:
2,3,4,5-tetra-O-acetyl-1-deoxy-1-(4,5-dimethyl-2-[(E)-(4-nitrophenyl)diazenyl]phenylamino)pentitol is utilized as a reagent in organic synthesis, serving as a key component in the preparation of more complex organic molecules. Its versatility in chemical reactions makes it a valuable asset in the synthesis of a wide range of compounds.
Used in Materials Science:
In the field of materials science, 2,3,4,5-tetra-O-acetyl-1-deoxy-1-(4,5-dimethyl-2-[(E)-(4-nitrophenyl)diazenyl]phenylamino)pentitol is recognized for its potential in the development of functional dyes. The presence of the azo and nitro groups in its structure contributes to its color and light-sensitive properties, which are essential for dye applications.
Used in Photochemistry:
2,3,4,5-tetra-O-acetyl-1-deoxy-1-(4,5-dimethyl-2-[(E)-(4-nitrophenyl)diazenyl]phenylamino)pentitol is also employed in photochemistry, where its light-sensitive azobenzene moiety can undergo reversible trans-cis isomerization upon exposure to light. This property makes it a candidate for applications in optical switches and molecular sensors, where light-induced changes in molecular structure can be harnessed for various purposes.
Used in Polymer Photostabilization:
2,3,4,5-tetra-O-acetyl-1-deoxy-1-(4,5-dimethyl-2-[(E)-(4-nitrophenyl)diazenyl]phenylamino)pentitol is used as a photostabilizer for polymers, where its ability to absorb light and dissipate energy can help protect polymer materials from the degrading effects of UV radiation. This application is particularly relevant in industries that rely on the durability and longevity of plastic materials exposed to sunlight, such as the automotive and construction sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 6973-44-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6973-44:
(6*6)+(5*9)+(4*7)+(3*3)+(2*4)+(1*4)=130
130 % 10 = 0
So 6973-44-0 is a valid CAS Registry Number.

6973-44-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [2,3,4-triacetyloxy-5-[4,5-dimethyl-2-[(4-nitrophenyl)diazenyl]anilino]pentyl] acetate

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

Emergency phone number -
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More Details:6973-44-0 SDS

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