65924-65-4

Basic information

• Product Name: 2-(TERT-BUTYLTHIO)BENZALDEHYDE
• Synonyms: 2-(TERT-BUTYLTHIO)BENZALDEHYDE;2-(tert-butylmercapto)benzaldehyde;Benzaldehyde, 2-[(1,1-dimethylethyl)thio]-
• CAS NO: 65924-65-4
• Molecular Formula: C₁₁H₁₄OS
• Molecular Weight: 194.29
• Mol File: 65924-65-4.mol
• Article Data: 19

Chemical Properties

• Boiling Point: 95-97°C 0,1mm
• Flash Point: 95-97°C/0.1mm
• Appearance: /
• Density: 1.05g/cm³
• Vapor Pressure: 0.003mmHg at 25°C
• Refractive Index: 1.547
• CAS DataBase Reference: 2-(TERT-BUTYLTHIO)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(TERT-BUTYLTHIO)BENZALDEHYDE(65924-65-4)
• EPA Substance Registry System: 2-(TERT-BUTYLTHIO)BENZALDEHYDE(65924-65-4)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 65924-65-4(Hazardous Substances Data)

Usage

General Description

2-(tert-butylthio)benzaldehyde is a chemical compound with the molecular formula C11H16OS. It is an aromatic aldehyde that contains a tert-butylthio group, which is a thioether with a tert-butyl substituent. 2-(TERT-BUTYLTHIO)BENZALDEHYDE is commonly used as a fragrance and flavoring agent in the production of perfumes and other scented products. It is also utilized in the synthesis of organic compounds and pharmaceuticals. Additionally, 2-(tert-butylthio)benzaldehyde has been studied for its potential antimicrobial and insecticidal properties, making it a versatile and useful chemical in various industrial and scientific applications.

InChI:InChI=1/C11H14OS/c1-11(2,3)13-10-7-5-4-6-9(10)8-12/h4-8H,1-3H3

Upstream product

• 75-66-1 2-methylpropan-2-thiol 
• 552-89-6 2-nitro-benzaldehyde 
• 127787-14-8 N-(Bis-trimethylsilanyl-methyl)-2-tert-butylsulfanyl-N-methyl-benzamide 
• 89-98-5 2-chloro-benzaldehyde 
• 127787-04-6 N-(Bis-trimethylsilanyl-methyl)-N-methyl-benzamide 
• 611-74-5 N,N-dimethylbenzamide 
• 446-52-6 2-Fluorobenzaldehyde 
• 29364-29-2 sodium tert-butyl thiolate 
• 6630-33-7 ortho-bromobenzaldehyde 

Downstream Products

• 117194-85-1 (E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-diethylamino-ethyl)-acrylamide 
• 115-11-7 isobutene 
• 123746-54-3 N,N'-bis(o-tert-butylthiobenzyliden)ethylenediamine 
• 117194-86-2 (E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-morpholin-4-yl-ethyl)-acrylamide 
• 117194-84-0 (E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-dimethylamino-ethyl)-acrylamide 
• 138248-76-7 2-{[1-(2-tert-Butylsulfanyl-phenyl)-meth-(E)-ylidene]-amino}-4-methylsulfanyl-butyramide 
• 55164-16-4 2,2'-dithiodibenzaldehyde 
• 100790-00-9 2-(2-methylpropane-2-sulfinyl)benzaldehyde 
• 181418-96-2 2-amino-3,5-dicyano-6-ethoxy-4-(2-tert-butylthiolphenyl)pyridine 
• 216986-33-3 2-(2-tert-butythiophenyl)benzothiazolidine 
• 623549-03-1 bis[2-(tert-butylthio)benzyl](2-pyridylmethyl)amine 
• 765292-68-0 2-[2'-(tert-butylsulfanyl)phenyl]-1,3-dithiane 

Relevant articles and documents

Palladium-Catalyzed Domino Cyclization/Phosphorylation of gem-Dibromoolefins with P(O)H Compounds: Synthesis of Phosphorylated Heteroaromatics

We presented a palladium-catalyzed domino cyclization/phosphorylation of gem-dibromoolefins, which utilize H-phosphinates and secondary phosphine oxides as the phosphine sources, respectively. A variety of phosphorylated heteroaromatics were obtained in m

Fabrication of egg shell-like nanovesicles from a thiocoumarin-based ?-amino ester: A potential carrier

Nanoscale egg shell-like drug delivery systems from methyl 6-amino-2-oxo-2H-thiochromene-3-carboxylate, a thiocoumarin-based ?-amino ester, have been investigated as potential candidates for drug delivery vehicles. X-ray crystallography reveals that the ?

Preparation of 4,7-dibromobenzo[b]thiophene as a versatile building block and synthetic application to a bis(ethynylthienyl)oligoarene system

Benzo[b]thiophene, 4,7-dibromobenzo[b]thiophene, thieno[3,2-b]thiophene, and 3-bromothieno[3,2-b]thiophene were prepared by AuCl-catalyzed cyclization of (t-butylsulfanyl)(ethynyl)benzenes or (t-butylsulfanyl)(ethynyl)thiophenes. Several reactions of 4,7-dibromobenzo[b]thiophene were investigated, including metallation and cross coupling reactions.