1756-31-6

Basic information

• Product Name: 1-(3,5-di-tert-butylphenyl)ethanone
• Synonyms: 1-(3,5-di-tert-butylphenyl)ethanone
• CAS NO: 1756-31-6
• Molecular Formula: C₁₆H₂₄O
• Molecular Weight: 232.36116
• Mol File: 1756-31-6.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 267.035 °C at 760 mmHg
• Flash Point: 102.137 °C
• Appearance: /
• Density: 0.914 g/cm³
• CAS DataBase Reference: 1-(3,5-di-tert-butylphenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3,5-di-tert-butylphenyl)ethanone(1756-31-6)
• EPA Substance Registry System: 1-(3,5-di-tert-butylphenyl)ethanone(1756-31-6)

Safety Data

• Hazardous Substances Data: 1756-31-6(Hazardous Substances Data)

Usage

Description

1-(3,5-di-tert-butylphenyl)ethanone is a chemical compound with the molecular formula C16H22O. It is a pale yellow liquid known for its strong and long-lasting pleasant aroma.

Uses

Used in Food and Beverage Industry:
1-(3,5-di-tert-butylphenyl)ethanone is used as a flavoring agent for adding a pleasant taste and aroma to various food and beverage products.
Used in Perfume and Fragrance Industry:
1-(3,5-di-tert-butylphenyl)ethanone is used as a key ingredient in the production of perfumes and fragrances due to its strong and long-lasting scent.
Used in Pharmaceutical Industry:
1-(3,5-di-tert-butylphenyl)ethanone is used in the pharmaceutical industry for its potential applications in creating medicinal compounds and formulations.
Used in Cosmetic Industry:
1-(3,5-di-tert-butylphenyl)ethanone is used in the cosmetic industry for adding fragrance to various cosmetic products such as lotions, creams, and perfumes.
It is important to handle 1-(3,5-di-tert-butylphenyl)ethanone with care, as it can be harmful if ingested or inhaled, and can cause irritation to the skin and eyes.

Upstream product

• 1460-02-2 1,3,5-Tri-tert-butylbenzene 
• 75-36-5 acetyl chloride 
• 1012-76-6 di-tert-butylbenzene 
• 1012-72-2 1,4-di-tert-butylbenzene 
• 917-54-4 methyllithium 
• 16225-26-6 3,5-di-tert-butylbenzoic acid 
• 75-15-0 carbon disulfide 
• 7446-70-0 aluminium trichloride 
• 36720-94-2 1,3-di-tert-butyl-5-ethynylbenzene 
• 14377-33-4 3,5-di-tert-butylbenzoyl chloride 
• 1207204-53-2 (+/-)-1-(3,5-di-tert-butylphenyl)ethanol 
• 22385-77-9 1-bromo-3,5-di-tert-butylbenzene 
• 97674-02-7 tributyl(1-ethoxyvinyl)stannane 
• 408311-46-6 2,2'-o-Phenylen-di-<2,2-dimethyl-aethanol-(1)>-di-(butylthioaether) 

Downstream Products

• 74128-92-0 2-(3,5-Di-tert-butylphenyl)-N,N-dimethyl-2-oxoessigsaeurethioamid 
• 178688-24-9 (Z)-3-(3,5-Di-tert-butyl-phenyl)-but-2-enenitrile 
• 178688-23-8 (E)-3-(3,5-Di-tert-butyl-phenyl)-but-2-enenitrile 
• 16225-26-6 3,5-di-tert-butylbenzoic acid 
• 5723-95-5 Essigsaeure-(3,5-di-tert.-butyl-phenylester) 
• 1351169-37-3 (E)-methyl 2-(3-aminopropoxy)-4-[3-(3,5-di-tertbutylphenyl)-3-oxoprop-1-enyl]benzoate hydrochloride 
• 1351169-36-2 (E)-methyl 2-[3-(tert-butoxycarbonylamino)propoxy]-4-[3-(3,5-di-tert-butylphenyl)-3-oxoprop-1-enyl]benzoate 
• 1351169-35-1 (E)-methyl 4-[3-(3,5-di-tert-butylphenyl)-3-oxoprop-1-enyl]-2-hydroxybenzoate 
• 1351169-34-0 C₂₅H₃₁BrO₄ 
• 1351169-33-9 C₂₆H₃₂O₄ 
• 1351169-32-8 diethyl 3,5-di-tert-butylbenzoylmethylphosphonate 
• 1351169-28-2 (S,E)-4-[3-(3,5-di-tert-butylphenyl)-3-oxoprop-1-enyl]-2-(3-{2-[2-(2-{2-[4-methyl-2-(4-phenylbutanamido)pentanamido]ethoxy}ethoxy)ethoxy]acetamido}propoxy)benzoic acid 
• 1351169-43-1 (S,E)-methyl 4-[3-(3,5-di-tert-butylphenyl)-3-oxoprop-1-enyl]-2-(3-{2-[2-(2-{2-[4-methyl-2-(4-phenylbutanamido)pentanamido]ethoxy}ethoxy)ethoxy]acetamido}propoxy)benzoate 
• 1351169-27-1 2-[3-(2-{2-[2-(2-{(S)-2-[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanamido]-4-methylpentanamido}ethoxy)ethoxy]ethoxy}acetamido)propoxy]-4-[(E)-3-(3,5-di-tert-butylphenyl)-3-oxoprop-1-enyl]benzoic acid 

Relevant articles and documents

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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).

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