7743-94-4 Usage
Uses
Used in Surface Coating Industry:
(2-Ethoxyethoxy)acetic acid is used as a component in surface coatings for its ability to improve the adhesion and durability of the final product.
Used in Adhesive Industry:
In the adhesive industry, (2-Ethoxyethoxy)acetic acid is used as a component to enhance the bonding strength and flexibility of adhesives.
Used in Cleaning Products Industry:
(2-Ethoxyethoxy)acetic acid is used as an ingredient in cleaning products for its ability to dissolve and remove various types of dirt and stains.
Used as a Solvent in Chemical Processes:
(2-Ethoxyethoxy)acetic acid is used as a solvent in various chemical processes due to its ability to dissolve a wide range of substances and facilitate chemical reactions.
Used as a Raw Material in Chemical Synthesis:
(2-Ethoxyethoxy)acetic acid is used as a raw material in the synthesis of other chemical compounds, contributing to the production of various industrial and consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 7743-94-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,4 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7743-94:
(6*7)+(5*7)+(4*4)+(3*3)+(2*9)+(1*4)=124
124 % 10 = 4
So 7743-94-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O4/c1-2-9-3-4-10-5-6(7)8/h2-5H2,1H3,(H,7,8)
7743-94-4Relevant academic research and scientific papers
ANDROGEN RECEPTOR MODULATORS AND METHOD OF TREATING DISEASE USING THE SAME
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Page/Page column 104, (2010/02/14)
Disclosed herein are bicycloaryl compounds of Formula (I) that selectively modulate nuclear receptors, preferably the androgen receptor, or a pharmaceutically acceptable salt, ester, amide, or prodrug thereof, and methods of treating disease comprising administering a compound of Formula (I) to a patient in need thereof.
Preparation of naphthoquinone derivatives from plumbagin and their ichthyotoxicity
Ogihara, Kazuhito,Yamashiro, Rieko,Higa, Matsutake,Yogi, Seiichi
, p. 437 - 445 (2007/10/03)
Various naphthoquinone derivatives were prepared from a natural product, 5-hydroxy-2-methyl-1,4-naphthoquinone (plumbagin); these were mostly substituted at C-3 through carbon-carbon bond formation mediated by a metal- based oxidant such as lead tetraacetate in the presence of various carboxylic acids. The halogenated compounds showed stronger ichthyotoxicity than plumbagin, but other derivatives were less active.
