14734-25-9

Basic information

• Product Name: TERT-BUTYL METHYL SUCCINATE 97
• Synonyms: TERT-BUTYL METHYL SUCCINATE 97;tert-Butyl methyl succinate 97%
• CAS NO: 14734-25-9
• Molecular Formula: C₉H₁₆O₄
• Molecular Weight: 188.221
• Product Categories: C8 to C9;Carbonyl Compounds;Esters;Building Blocks;C8 to C9;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks
• Mol File: 14734-25-9.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 85-95 °C20 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 1.022 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.301mmHg at 25°C
• Refractive Index: n20/D 1.421(lit.)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: TERT-BUTYL METHYL SUCCINATE 97(CAS DataBase Reference)
• NIST Chemistry Reference: TERT-BUTYL METHYL SUCCINATE 97(14734-25-9)
• EPA Substance Registry System: TERT-BUTYL METHYL SUCCINATE 97(14734-25-9)

Safety Data

• Safety Statements: 23-24/25
• WGK Germany: 3
• RTECS: MO1360000
• Hazardous Substances Data: 14734-25-9(Hazardous Substances Data)

Usage

Description

TERT-BUTYL METHYL SUCCINATE 97, also known as tert-butyl methyl succinate, is an ester compound derived from the addition reaction between tert-butyl alcohol and 4-oxo-but-3-enoate in the presence of lithium tert-butoxide as a catalyst. It exists as a mixture of its threoand erythroisomeric forms and is known for its unique chemical properties and potential applications in various industries.

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

• 15026-17-2 succinic acid mono-tert-butyl ester 
• 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 
• 97218-68-3 (R)-4-Hydroxy-5-((R)-toluene-4-sulfinyl)-pentanoic acid tert-butyl ester 
• 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 

Relevant articles and documents

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.

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.

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