41828-13-1

Usage

Uses

Used in Pharmaceutical Industry:
Tetralin-1-carbaldehyde is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicinal compounds.
Used in Food Industry:
As a flavoring agent, tetralin-1-carbaldehyde is utilized for its pleasant floral scent, enhancing the aroma of various food products.
Used in Perfume and Fragrance Industry:
Tetralin-1-carbaldehyde is employed as an aromatic ingredient in perfumes and fragrances, adding a floral note to these products.
Used in Agrochemical Production:
tetralin-1-carbaldehyde serves as a versatile intermediate in the production of agrochemicals, playing a role in the development of agricultural products.
Used in Dye Production:
Tetralin-1-carbaldehyde is used in the manufacturing process of dyes, contributing to the coloration and properties of various dye products.

InChI:InChI=1/C11H12O/c12-8-10-6-3-5-9-4-1-2-7-11(9)10/h3,5-6,8H,1-2,4,7H2

Upstream product

• 119-64-2 tetralin 
• 201230-82-2 carbon monoxide 
• 116451-84-4 (2E,9E)-Undeca-2,9-dienedial 
• 4885-02-3 Dichloromethyl methyl ether 

Downstream Products

• 104778-46-3 5-fluoro-3-(5,6,7,8-tetrahydro-1-naphthalenyl)-1(3H)-isobenzofuranone 
• 41790-30-1 (5,6,7,8-tetrahydronaphthalene-1-yl)methanol 
• 856198-59-9 (+/-)-Hydroxy-phenyl-(5.6.7.8-tetrahydro-naphthyl-⁽¹⁾)-methan 
• 776-50-1 (1,2,3,4-tetrahydro-5-naphthyl)acetic acid 
• 3160-17-6 2-(5,6,7,8-tetrahydronaphthalene-1-yl)acetonitrile 
• 1478-33-7 6-fluoro-2-<(5,6,7,8-tetrahydro-1-naphthalenyl)methyl>benzoic acid 
• 1187976-31-3 (4,5-dihydrothiazol-2-yl)-[2-(3,5-dimethylphenyl)-1-(5,6,7,8-tetrahydronaphthalen-1-yl)-ethyl]-amine 
• 1187976-34-6 1-[2-(3,5-dimethylphenyl)-1-(5,6,7,8-tetrahydronaphthalen-1-yl)-ethyl]-3-(2-hydroxyethyl)-thiourea 
• 1187976-32-4 2-(3,5-dimethylphenyl)-1-(5,6,7,8-tetrahydronaphthalen-1-yl)-ethylamine 
• 75489-92-8 4-(5,6,7,8-tetrahydro-[1]naphthyl)-butyric acid 
• 104761-67-3 4-fluoro-2-<(5,6,7,8-tetrahydro-1-naphthalenyl)methyl>benzoic acid 
• 35310-83-9 phenyl(5,6,7,8-tetrahydronaphthalen-1-yl)methanone 
• 4242-18-6 5,6,7,8-tetrahydro-1-naphthalenecarboxylic acid 

Relevant academic research and scientific papers

BCL-2 INHIBITOR

Disclosed herein is a compound of Formula (I) for inhibiting both Bcl-2 wild type and mutated Bcl-2, in particular, Bcl-2 G101V and D103Y, and a method of using the compound disclosed herein for treating dysregulated apoptotic diseases.

Synthesis of aromatic aldehydes by organocatalytic [4+2] and [3+3] cycloaddition of α,β-unsaturated aldehydes

Organocatalytic inter- and intramolecular [4+2] and [3+3] cycloadditions of α,β-unsaturated aldehydes to give polysubstituted aromatic aldehydes are described. High periselectivity for the cycloadditions, with catalyst effects exerted by l-proline and pyrrolidine-HOAc, as well as cocatalyst, additive effects, has been observed.

Formylation of Aromatic Compounds with CO in HSO3F-SbF5 under Atmospheric Pressure

The formylation of aromatic compounds such as benzene, toluene, xylenes, mesitylene, indan, tetralin, fluorobenzene, chlorobenzene, and bromobenzene was carried out in HSO3F-SbF5 under atmospheric CO pressure at 0 deg C.In HSO3F-SbF5, both formylation and sulfonation took place to give formyl and sulfonyl compounds.In the case of alkylbenzenes, including toluene, xylenes, mesitylene, and tetralin, formylalkylbenzenesulfonyl fluorides, new compounds, were obtained by a one-pot reaction as well as alkylbenzaldehydes, alkylbenzenesulfonyl fluorides, and bis(alkylphenyl) sulfones.The direct introduction of a formyl and sulfonyl group was achieved in alkylbenzenes.The reaction path of the new compounds is a two-step reaction comprised of formylation as the first step and sulfonation as the second step.The product composition was strongly dependent on the acid strength of the HSO3F-SbF5 systems.The formyl compounds became predominant with increasing acidity of the HSO3F-SbF5 system.On the other hand, only sulfonyl compounds were produced when the acidity of the HSO3F-SbF5 system was low.