1005738-28-2

Basic information

• Product Name: C₁₂H₁₂O₈S
• Synonyms: C₁₂H₁₂O₈S
• CAS NO: 1005738-28-2
• Molecular Weight: 316.288
• Mol File: 1005738-28-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₁₂H₁₂O₈S(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₂H₁₂O₈S(1005738-28-2)
• EPA Substance Registry System: C₁₂H₁₂O₈S(1005738-28-2)

Safety Data

• Hazardous Substances Data: 1005738-28-2(Hazardous Substances Data)

Upstream product

• 99-10-5 3,5-Dihydroxybenzoic acid 
• 35354-29-1 3,5-diacetoxybenzoic acid 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 1236211-46-3 5-(4-acetoxyphenylcarbamoyl)-1,3-phenylene Diacetate 
• 926294-00-0 3,5-dihydroxy-N-(3-hydroxyphenyl)benzamide 
• 890978-08-2 5-(4-hydroxyphenylcarbamoyl)-1,3-phenylene diacetate 

Relevant articles and documents

The application of template selectophores for the preparation of molecularly imprinted polymers

Molecularly imprinted polymers are versatile materials with wide application scope for the detection, capture and separation of specific compounds present in complex feed stocks. A major challenge associated with their preparation has been the need to sacrifice one mole equivalent of the template molecule to generate the complementary polymer cavities that selectively bind the target molecule. Moreover, template molecules can often be difficult to synthesise, expensive or lack stability. In this study, we describe a new approach, directed at the use of synthetic selectophores, chosen as readily prepared and low cost structural analogues with recognition groups in similar three-dimensional arrangements as found in the target molecule. To validate the approach, a comparative study of selectophores related to the polyphenolic compound (E)-resveratrol has been undertaken using traditional and green chemical synthetic approaches. These molecular mimic compounds were employed as polymer templates and also as binding analytes to interrogate the recognition sites associated with the molecularly imprinted polymers. Importantly, the study confirms that the use of selectophores has the potential to confer practical advantages, including access to more efficient methods for selection and preparation of suitable template molecules with a broader range of molecular diversity, as well as delivering imprinted polymers capable of recognizing the target compound and structurally related products.

HYDROXYBENZAMIDE DERIVATIVES, THE METHOD FOR PREPARING THEREOF AND THE COSMETIC COMPOSITION CONTAINING THE SAME

Disclosed is a hydroxybenzamide derivative represented by the following Formula (1). A method for preparing the same and a cosmetic composition comprising the same are also disclosed. More particularly, the hydroxybenzamide derivative is obtained by react