64277-87-8

Basic information

• Product Name: 3,5-DI-TERT-BUTYLBENZOIC ACID METHYL ESTER
• Synonyms: METHYL 3,5-DI-TERT-BUTYLBENZOATE;3,5-DI-TERT-BUTYLBENZOIC ACID METHYL ESTER;RARECHEM AL BF 0560;Methyl 3,5-Di-tert-butylbenzoate
• CAS NO: 64277-87-8
• Molecular Formula: C₁₆H₂₄O₂
• Molecular Weight: 248.36
• Product Categories: Building Blocks for Dendrimers;Functional Materials
• Mol File: 64277-87-8.mol
• Article Data: 8

Chemical Properties

• Melting Point: 53 °C
• Boiling Point: 303.5°C at 760 mmHg
• Flash Point: 136.7°C
• Appearance: /
• Density: 0.952g/cm³
• Vapor Pressure: 0.000926mmHg at 25°C
• Refractive Index: 1.485
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3,5-DI-TERT-BUTYLBENZOIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DI-TERT-BUTYLBENZOIC ACID METHYL ESTER(64277-87-8)
• EPA Substance Registry System: 3,5-DI-TERT-BUTYLBENZOIC ACID METHYL ESTER(64277-87-8)

Safety Data

• Hazardous Substances Data: 64277-87-8(Hazardous Substances Data)

Usage

General Description

3,5-Di-tert-butylbenzoic acid methyl ester is a chemical compound that is used in various industrial applications. It is a derivative of benzoic acid and is typically used as a flavoring agent in the food industry. It is also used as a stabilizer in plastics and polymers, as well as a fragrance ingredient in cosmetics and personal care products. Additionally, it has potential applications in pharmaceuticals and agricultural chemicals. The compound is known for its strong, stable structure and its ability to enhance the performance and longevity of various materials and products. It is considered to be relatively safe for use and handling, with low toxicity and minimal environmental impact.

InChI:InChI=1/C16H24O2/c1-15(2,3)12-8-11(14(17)18-7)9-13(10-12)16(4,5)6/h8-10H,1-7H3

Upstream product

• 67-56-1 methanol 
• 16225-26-6 3,5-di-tert-butylbenzoic acid 
• 17610-00-3 3,5-Di-tert-butylbenzaldehyde 
• 124-41-4 sodium methylate 
• 100-52-7 benzaldehyde 
• 74-88-4 methyl iodide 
• 15181-11-0 3, 5-di-tert-butyltoluene 

Downstream Products

• 77387-57-6 3,5-bis(1,1-dimethylethyl)benzenemethanol 
• 85313-49-1 t-Bumeoc-Trp-OH 
• 85313-53-7 t-Bumeoc-Lys(N-Boc)-OH*DCHA 
• 85313-58-2 t-Bumeoc-L-Phe-D-Leu-L-Arg-L-Phe-NH₂ 
• 85313-48-0 t-Bumeoc-Ser-(t-Bu)-OH*DCHA 
• 85313-43-5 t-Bumeoc-D-Leu*DCHA 
• 85313-51-5 t-Bumeoc-Val-OH*DCHA 
• 85313-56-0 t-Bumeoc-L-Phe-D-Leu-OH 
• 85313-54-8 t-Bumeoc-L-Phe-Gly-OMe 
• 85313-44-6 t-Bumeoc-L-Phe-OH 
• 85313-46-8 t-Bumeoc-Gln 
• 85313-45-7 t-Bumeoc-Gly-OEt 
• 85313-41-3 t-Bumeoc-Ala-OH 

Relevant articles and documents

Organoiridium complex for organic electroluminescent elements

The present invention provides an organometallic complex having a high quantum efficiency even in a polymer thin film as a emitting material for organic electroluminescent (EL) element. The present invention relates to an organoiridium complex for an organic electroluminescent element represented by the following Formula; wherein a C—N ligand including two atomic groups (A1, A2), and a β-diketone ligand in line symmetry having two tert-butyl-substituted phenyl groups are coordinated with an iridium atom. The organoiridium complex of the present invention has a high quantum efficiency even in a polymer thin film with respect to green to yellow electroluminescence. (In the aforementioned Formula, R1, R2, and R3 are each a tert-butyl group or a hydrogen atom, and have at least one tert-butyl group; they may bond each other to thereby form a saturated hydrocarbon ring, when having two tert-butyl groups; A1, A2 are each an unsaturated hydrocarbon ring, at least one is a single ring, and at least one is a heterocyclic ring).

Size-Selective Yolk-Shell Nanoreactors with Nanometer-Thin Porous Polymer Shells

Yolk-shell nanoreactors with metal nanoparticle core and ultrathin porous polymer shells are effective catalysts for heterogeneous reactions. Polymer shells provide size-selectivity and improved reusability of catalyst. Nanocapsules with single-nanometer porous shells are prepared by vesiclelated directed assembly. Metal nanoparticles are formed either by selective initiation in pre-fabricated nanocapsules or simultaneously with the creation of a crosslinked polymer shell. In this study, we investigated the oxidation of benzyl alcohol and benzaldehyde catalyzed by gold nanoparticles and hydrogenation of cyclohexene catalyzed by platinum nanoparticles. Comparison of newly created nanoreactors with commercially available nanoparticles revealed superior reusability and size selectivity in nanoreactors while showing no negative effect on reaction kinetics.

High comonomer selectivity in ethylene/hexene copolymerization by unbridged indenyl metallocenes

Catalysts derived from unbridged 2-arylindene metallocenes of Hf and Zr are active for ethylene/hexene copolymerization and show a much higher selectivity toward hexene than unsubstituted bis(indenyl) metallocenes. The ligand substitution pattern and the