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18791-79-2

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18791-79-2 Usage

General Description

2-Bromothiophen-4-aldehyde is a chemical compound that is commonly used in the synthesis of pharmaceuticals, agrochemicals, and dyes. It is a member of the thiophene family, which are heterocyclic compounds containing sulfur. 2-BROMOTHIOPHEN-4-ALDEHYDE is known for its aromatic and reactive properties, making it a useful building block in organic synthesis. 2-Bromothiophen-4-aldehyde is also used in the production of various fragrances and flavors due to its distinct odor. Additionally, this compound has potential applications in the development of novel materials and as a reagent in organic chemistry reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 18791-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,9 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18791-79:
(7*1)+(6*8)+(5*7)+(4*9)+(3*1)+(2*7)+(1*9)=152
152 % 10 = 2
So 18791-79-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H3BrOS/c6-5-1-4(2-7)3-8-5/h1-3H

18791-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromothiophene-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-Bromothiophene-3-carboxaldehyde

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:18791-79-2 SDS

18791-79-2Relevant articles and documents

New donor-acceptor benzotrithiophene-containing conjugated polymers for solar cells

Keshtov,Kuklin,Kochurov,Konstantinov,Krayushkin,Radychev,Khokhlov

, p. 25 - 31 (2014)

-

ISOXAZOLIDINES AS RIPK1 INHIBITORS AND USE THEREOF

-

Page/Page column 193, (2021/12/31)

The present invention relates to isoxazolidines of formula I and their use as receptor-interacting protein kinase 1 inhibitors, for example in the treatment of diseases and disorders mediated by RIP kinase (1) such as rheumatoid arthritis (RA), psoriasis, inflammatory bowel disease (IBD), Crohn's disease or ulcerative colitis.

In-flow photooxygenation of aminothienopyridinones generates iminopyridinedione PTP4A3 phosphatase inhibitors

Tasker, Nikhil R.,Rastelli, Ettore J.,Blanco, Isabella K.,Burnett, James C.,Sharlow, Elizabeth R.,Lazo, John S.,Wipf, Peter

supporting information, p. 2448 - 2466 (2019/03/06)

A continuous flow photooxygenation of 7-aminothieno[3,2-c]pyridin-4(5H)-ones to produce 7-iminothieno[3,2-c]pyridine-4,6(5H,7H)-diones has been developed, utilizing ambient air as the sole reactant. N-H Imines are formed as the major products, and excellent functional group tolerance and conversion on gram-scale without the need for chromatographic purification allow for facile late-stage diversification of the aminothienopyridinone scaffold. Several analogs exhibit potent in vitro inhibition of the cancer-associated protein tyrosine phosphatase PTP4A3, and the SAR supports an exploratory docking model.

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