879015-64-2

Basic information

• Product Name: 1-Propanol, 3-(2-propenyloxy)-2,2-bis[(2-propenyloxy)methyl]-, 4-methylbenzenesulfonate
• CAS NO: 879015-64-2
• Molecular Formula: C21H30O6S
• Molecular Weight: 410.532
• Mol File: 879015-64-2.mol

Chemical Properties

• CAS DataBase Reference: 1-Propanol, 3-(2-propenyloxy)-2,2-bis[(2-propenyloxy)methyl]-, 4-methylbenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanol, 3-(2-propenyloxy)-2,2-bis[(2-propenyloxy)methyl]-, 4-methylbenzenesulfonate(879015-64-2)
• EPA Substance Registry System: 1-Propanol, 3-(2-propenyloxy)-2,2-bis[(2-propenyloxy)methyl]-, 4-methylbenzenesulfonate(879015-64-2)

Safety Data

• Hazardous Substances Data: 879015-64-2(Hazardous Substances Data)

Usage

Epoxy resin

1-Propanol, 3-(2-propenyloxy)-2,2-bis[(2-propenyloxy)methyl]-, 4-methylbenzenesulfonate is a type of epoxy resin, which is a polymer formed by the reaction of an epoxy compound with a hardener.

Crosslinking agent

1-Propanol, 3-(2-propenyloxy)-2,2-bis[(2-propenyloxy)methyl]-, 4-methylbenzenesulfonate is commonly used as a crosslinking agent, which helps to strengthen and improve the durability of polymers and resins by forming a three-dimensional network between polymer chains.

Upstream product

• 1471-17-6 pentaerythritol triallyl ether 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 882516-57-6 tri-O-(2-acetoxyethyl)-O-tosylpentaerythritol 
• 879015-68-6 5-[(p-iodophenoxy)methyl]-5-[(2-hydroxyethoxy)methyl]-3,7-dioxa-1,9-nonanediol 
• 879015-67-5 5-[(p-bromophenoxy)methyl]-5-[(2-hydroxyethoxy)methyl]-3,7-dioxa-1,9-nonanediol 
• 882516-56-5 tri-O-(2-hydroxyethyl)-O-tosylpentaerythritol 
• 879015-66-4 1,3-bis(allyloxy)-2-allyloxymethyl-2-[(p-iodophenoxy)methyl]propane 
• 879015-65-3 1,3-bis(allyloxy)-2-allyloxymethyl-2-[(p-bromophenoxy)methyl]propane 

Relevant articles and documents

Synthesis of a nonavalent mannoside glycodendrimer based on pentaerythritol

A nonavalent glycodendrimer bearing terminal α-D-mannopyranoside units has been synthesized with a convergent approach. Terminal trivalent mannoside dendrons bearing p-halophenyl ethers were prepared by glycosylation of pentaerythritol derivatives having

Synthesis of cluster mannosides carrying a photolabile diazirine group

We are investigating the mechanisms underlying the carbohydrate-specific adhesion of bacteria such as Escherichia coli to the glycocalyx of their potential host cells. E. coli possess protein appendages, which are called type 1 fimbriae. Part of type 1 fimbriae is a protein named FimH, which is a mannose-specific lectin. We wish to use photoaffinity labeling to elucidate mannose binding sites on FimH. Thus we report the synthesis of di- and trivalent cluster mannosides, which carry a photolabile diazirine group. The diazirine group was introduced by a convergent approach using thiourea bridging (products 6, 13, 17, and 27) or in a divergent synthesis leading to the divalent cluster mannoside 31. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.