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4,6-Dichloro-2H-1-benzothiine-3-carbaldehyde is a chemical compound characterized by its molecular formula C9H5Cl2OS. It presents as a yellowish solid with a distinct odor and is primarily utilized in the pharmaceutical and agrochemical industries. 4,6-DICHLORO-2H-1-BENZOTHIINE-3-CARBALDEHYDE also serves as an intermediate in organic synthesis and is a common component in research and development. Due to its potential to cause irritation to the skin, eyes, and respiratory system, it is crucial to handle 4,6-Dichloro-2H-1-benzothiine-3-carbaldehyde with care and to implement proper safety measures during its use.

54949-15-4

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54949-15-4 Usage

Uses

Used in Pharmaceutical Industry:
4,6-DICHLORO-2H-1-BENZOTHIINE-3-CARBALDEHYDE is used as a key intermediate in the synthesis of various pharmaceutical compounds for its ability to contribute to the development of new drugs and enhance the properties of existing ones.
Used in Agrochemical Industry:
In the agrochemical sector, 4,6-DICHLORO-2H-1-BENZOTHIINE-3-CARBALDEHYDE is employed as a precursor in the production of agrochemicals, contributing to the formulation of pesticides and other agricultural chemicals that protect crops and enhance yield.
Used in Organic Synthesis:
4,6-DICHLORO-2H-1-BENZOTHIINE-3-CARBALDEHYDE is used as an intermediate in organic synthesis for its role in creating a variety of organic compounds, which can be further utilized in different chemical and industrial applications.
Used in Research and Development:
4,6-DICHLORO-2H-1-BENZOTHIINE-3-CARBALDEHYDE is also utilized in research and development settings, where it aids scientists in exploring new chemical reactions and developing innovative applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 54949-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,4 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54949-15:
(7*5)+(6*4)+(5*9)+(4*4)+(3*9)+(2*1)+(1*5)=154
154 % 10 = 4
So 54949-15-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H6Cl2OS/c11-7-1-2-9-8(3-7)10(12)6(4-13)5-14-9/h1-4H,5H2

54949-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-dichloro-2H-thiochromene-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names -

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:54949-15-4 SDS

54949-15-4Downstream Products

54949-15-4Relevant academic research and scientific papers

Design, synthesis, and biological evaluation of 4-chloro-2H-thiochromenes featuring nitrogen-containing side chains as potent antifungal agents

Wang, Dan-Jiao,Hou, Zhuang,Xu, Hang,An, Ran,Su, Xin,Guo, Chun

, p. 3574 - 3578 (2018/10/15)

A series of 4-chloro-2H-thiochromenes featuring nitrogen-containing side chains were designed, synthesized and tested in vitro for their antifungal activities. The results of preliminary antifungal tests showed that most target compounds exhibited good inhibitory activities against Candida albicans, Cryptococcus neoformans, Candida tropicalis. Notably, compounds 10e and 10y showed most potent activity in vitro against a variety of fungal pathogens with low MICs. Meanwhile, low cytotoxicity on mammalian cells has been observed for compounds 10e and 10y in the tested concentrations by the MTT assay. Therefore, the 4-chloro-2H-thiochromenes with nitrogen-containing groups provide new lead structures in the search for novel antifungal agents.

SUBSTITUTED SULFONE-CONTAINING TRICYCLIC COMPOUNDS AND USES THEREOF

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Page/Page column 32; 33, (2014/05/24)

The present invention relates to substituted sulfone-containing tricyclic compounds and analogues thereof which inhibit Bak-mediated apoptosis. The invention further relates to pharmaceutical compositions comprising a compound of the present invention and to methods of inhibiting a Bak-mediated apoptotic pathway and Bak-mediated apoptosis in a cell.

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