14734-25-9

Usage

Uses

Used in Chemical Synthesis:
TERT-BUTYL METHYL SUCCINATE 97 is used as an intermediate in the synthesis of various organic compounds for [application reason], such as pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique ester structure and reactivity make it a valuable building block in the development of new molecules with specific properties and functions.
Used in Polymer Industry:
In the polymer industry, TERT-BUTYL METHYL SUCCINATE 97 is used as a monomer for the production of polymers with specific properties, such as improved flexibility, toughness, or chemical resistance. Its incorporation into polymer chains can lead to the development of novel materials with enhanced performance characteristics for various applications.
Used in Lubricant Formulation:
TERT-BUTYL METHYL SUCCINATE 97 is used as an additive in the formulation of lubricants to improve their performance characteristics, such as reducing friction, enhancing load-carrying capacity, and providing better thermal stability. Its ester functionality can contribute to the overall performance of the lubricant, making it suitable for various industrial applications.
Used in Coatings and Adhesives:
In the coatings and adhesives industry, TERT-BUTYL METHYL SUCCINATE 97 is used as a component in the formulation of high-performance coatings and adhesives. Its unique chemical properties can contribute to improved adhesion, flexibility, and durability of the final product, making it suitable for various applications, such as automotive, construction, and consumer goods.
Used in Flavor and Fragrance Industry:
TERT-BUTYL METHYL SUCCINATE 97 can be used as a starting material in the synthesis of various flavor and fragrance compounds. Its unique chemical structure can be utilized to create novel aroma chemicals with specific scent profiles, contributing to the development of new and innovative products in the flavor and fragrance industry.

InChI:InChI=1/C9H16O4/c1-9(2,3)13-8(11)6-5-7(10)12-4/h5-6H2,1-4H3

Upstream product

• 75-65-0 tert-butyl alcohol 
• 1490-25-1 succinic acid monomethylester chloride 
• 67-56-1 methanol 
• 119060-47-8 tert-Butyl 2,2-dichlorocyclopropanecarboxylate 
• 96-32-2 bromoacetic acid methyl ester 
• 51656-70-3 (2-tert-butoxy-2-oxoethyl)zinc(II) bromide 
• 3878-55-5 methyl hydrogen succinate 
• 115-11-7 isobutene 
• 1663-39-4 tert-Butyl acrylate 

Downstream Products

• 115352-51-7 (R_S)-t-butyl-5-(4-methylphenyl)sulphinyl-4-oxo-decanoate 
• 97218-65-0 4-Oxo-5-((R)-toluene-4-sulfinyl)-pentanoic acid tert-butyl ester 
• 3878-55-5 methyl hydrogen succinate 
• 115352-59-5 (4R,5S)-t-butyl 4-hydroxy-5-(4-methylphenyl)thio decanoate 
• 115352-60-8 (-)-(4S,5S)-t-butyl 4-hydroxy-5-(4-methylphenyl)thio decanoate 
• 115405-25-9 (4S,5S,R_S)-t-butyl-5-(4-methylphenyl)sulphinyl decanoate 
• 115352-53-9 (+)-(4S,5R,R_S)-t-butyl-5-(4-methylphenyl)sulphinyl decanoate 
• 115405-24-8 (4R,5S,R_S)-t-butyl-5-(4-methylphenyl)sulphinyl decanoate 
• 115405-23-7 (4R,5R,R_S)-t-butyl-5-(4-methylphenyl)sulphinyl decanoate 
• 115352-58-4 (-)-(4S,5S)-t-butyl 4-benzyloxy-5-(4-methylphenyl)thio decanoate 
• 115352-57-3 (-)-(4R,5S)-t-butyl 4-benzyloxy-5-(4-methylphenyl)thio decanoate 
• 115405-28-2 (+)-(4S,5S,R_S)-t-butyl 4-benzyloxy-5-(4-methylphenyl)sulphinyl decanoate 
• 115352-55-1 (+)-(4R,5S,R_S)-t-butyl 4-benzyloxy-5-(4-methylphenyl)sulphinyl decanoate 
• 14734-22-6 3-(3-Carbo-t-butoxypropionyl)-malonsaeure-diethylester 

Relevant academic research and scientific papers

Low molecular weight peptide derivatives as inhibitors of the laminin/nidogen interaction

Low molecular weight peptide derivatives which are able to act as inhibitors of the interaction between laminin and nidogen (laminin/nidogen interaction), a process for their preparation, pharmaceutical compositions prepared therefrom and their use for preparing pharmaceuticals and for identifying inhibitors of the laminin/nidogen interaction.

Bisketene derivatives and process for production and use thereof

The novel 1,2-bisketene of Formula I: wherein:, R1 is SiR3R4R5;, R2 is selected from the group comprising SiR3R4R5, hydrogen, methyl, a substituted or unsubstituted C2 20linear or branched alkyl group, a substituted or unsubstituted C6 20 aryl group, a substituted or unsubstituted C5 20 cycloalkyl group and a halogen; and, each of R3, R4 and R5 are the same or different and are selected from the group comprising hydrogen, methyl, a substituted or unsubstituted C2 20 linear or branched alkyl group, a substituted or unsubstituted C6 20 aryl group, a substituted or unsubstituted C7 20 aralkyl group and substituted or unsubstituted a C5 20 cycloalkyl group, is useful in e.g. preparing a succinate ester, or in reacting with a polyfunctional alcohol or ester to produce a polyester or polyamide.

Reactions of Organic Anions; CXLIX. Reactions of gem-Dichlorocyclopropanes Containing an Electron-Withdrawing Substituent with Organic Anions Generated with Phase-Transfer Catalysis

gem-Dichlorocyclopropanes 1 react with C-H, O-H and S-H acids in the presence of concentrated sodium hydroxide solution and a phase-transfer catalyst to give gem-disubstituted cyclopropanes 2 or chain products 3 in 44-95percent yield.

CONFORMATION OF SUCCINIC ACID DERIVATIVES BY DOUBLE 13C-LABELLING

Three-bonded carbon/carbon couplings (3Jcc) are used, in conjunction with MM2 calculations, to examine conformational equilibria in several di-13C-labelled succinic acid derivatives.

SYNTHESIS OF THE (4S,5R)-5-HYDROXY-DECAN-4-OLIDE (L-FACTOR) AND OF THE (R)-DECAN-4-OLIDE FROM A CHIRAL SULPHOXIDE

The condensation of optically pure (+)-R-n-hexyl 4-methylphenyl sulphoxide (9) on the succinic diester (8) produced the 4-oxo-5-sulphinyl decanoate 10 which was selectively reduced to the corresponding 4-hydroxy-5-sulphinyl decanoates 11.Starting from the

A REFORMATSKY REAGENT. C-C BONDS FORMATION BY SUBSTITUTION REACTIONS

The ability of a C-metallated Reformatsky reagent to undergo substitution reactions with different bromides has been tested.