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6-Benzofurancarboxaldehyde, 2,3-dihydro(9CI) is an aromatic aldehyde chemical compound characterized by a benzofuran ring structure and the molecular formula C10H10O2. It is recognized for its strong and distinct odor, making it a valuable component in the creation of scented products. Moreover, its potential medicinal properties, such as antimicrobial and antifungal activities, have been a subject of study. However, due to its potential for skin, eye, and respiratory irritation, as well as its toxicity if ingested or inhaled in large amounts, careful handling is required.

55745-96-5

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55745-96-5 Usage

Uses

Used in Pharmaceutical Industry:
6-Benzofurancarboxaldehyde, 2,3-dihydro(9CI) serves as an essential intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure contributes to the development of new drugs with potential therapeutic applications.
Used in Fragrance Industry:
Leveraging its strong and distinct odor, 6-Benzofurancarboxaldehyde, 2,3-dihydro(9CI) is used as a fragrance ingredient in the production of perfumes, colognes, and other scented consumer products, enhancing their olfactory profiles.
Used in Organic Synthesis:
Beyond its applications in pharmaceuticals and fragrances, 6-Benzofurancarboxaldehyde, 2,3-dihydro(9CI) is utilized in the synthesis of other organic compounds, highlighting its versatility in organic chemistry.
Used in Antimicrobial and Antifungal Applications:
Research into the potential medicinal properties of 6-Benzofurancarboxaldehyde, 2,3-dihydro(9CI) has revealed its antimicrobial and antifungal activities, suggesting its use in applications requiring the inhibition of microbial growth, such as in preservatives or disinfectants.

Check Digit Verification of cas no

The CAS Registry Mumber 55745-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,4 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55745-96:
(7*5)+(6*5)+(5*7)+(4*4)+(3*5)+(2*9)+(1*6)=155
155 % 10 = 5
So 55745-96-5 is a valid CAS Registry Number.

55745-96-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydro-1-benzofuran-6-carboxaldehyde

1.2 Other means of identification

Product number -
Other names 2,3-dihydro-1-benzofuran-6-carbaldehyde

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:55745-96-5 SDS

55745-96-5Relevant academic research and scientific papers

SPIRO COMPOUNDS AS GLYCOSIDASE INHIBITORS

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, (2020/03/15)

Compounds of formula (I) wherein A, R, L, Z, Q1, Q2 and n have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

TETRAHYDRO-BENZOAZEPINE GLYCOSIDASE INHIBITORS

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, (2020/03/15)

Compounds of formula (I') wherein A, R1, R2, T1, T2, T3, T4, L, W, Z, R''', m and n have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

FUSED GLYCOSIDASE INHIBITORS

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, (2020/09/08)

Compounds of formula (I), wherein A, Z, E, R1, R2, m and n have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

Methods for treating neisseria gonorrhoeae infection with substituted 1,2-dihydro-2A,5,8A-triazaacenaphthylene-3,8-diones

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Page/Page column 119, (2020/07/21)

The present invention relates to methods for treating Neisseria Gonorrhoeae infection which comprises administering to a subject in need thereof novel 1,2-dihydro-2a,5,8a-triazaacenaphthylene-3,8-dione compounds: or pharmaceutically acceptable salts thereof and/or corresponding pharmaceutical compositions.

ANNULATED GLYCOSIDASE INHIBITORS

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, (2019/03/12)

Compounds of formula (I) wherein A, R, W1, W2, W3, W4, W5, W6, L, Q, Rx and u have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

LINEAR GLYCOSIDASE INHIBITORS

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, (2019/03/14)

Compounds of formula (I) wherein A, R, W, Q, L, n and m have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

OGA INHIBITOR COMPOUNDS

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Page/Page column 55, (2020/01/11)

The present invention relates to O-GlcNAc hydrolase (OGA) inhibitors. The invention is also directed to pharmaceutical compositions comprising such compounds, to processes for preparing such compounds and compositions, and to the use of such compounds and compositions for the prevention and treatment of disorders in which inhibition of OGA is beneficial, such as tauopathies, in particular Alzheimer's disease or progressive supranuclear palsy; and neurodegenerative diseases accompanied by a tau pathology, in particular amyotrophic lateral sclerosis or frontotemporal lobe dementia caused by C90RF72 mutations.

GLYCOSIDASE INHIBITORS

-

, (2017/09/15)

Compounds of formula (I) wherein A, R, W, Q, n and m have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

GLYCOSIDASE INHIBITORS

-

, (2017/09/15)

Compounds of formula (I) wherein A, R, W, Q, n and m have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

PROCESS FOR THE SEPARATION OF ENANTIOMERS OF PIPERAZINE DERIVATIVES

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, (2017/09/21)

The invention relates to a process for preparing either enantiomer of a compound of formula (I), wherein X, Y and n have the meaning given in claim 1, with high enantiomeric excess (e.e.), by chiral resolution in the presence of a non-racemic, chiral acid.

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