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885279-11-8

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885279-11-8 Usage

General Description

2-(2-Methoxy-phenyl)-thiazole-4-carbaldehyde is a chemical compound that possesses the structural characteristics of methoxyphenyl and thiazole groups. Its molecular formula is C12H9NOS2, indicating that it is made up of carbon, hydrogen, nitrogen, oxygen, and sulfur atoms. 2-(2-METHOXY-PHENYL)-THIAZOLE-4-CARBALDEHYDE finds its importance in research and study within the field of organic chemistry and it may have potential applications in drug development or materials science due to its specific molecular structure, though further investigation and verification are needed. Its properties will be dependent on variables such as temperature, pressure, and interactions with other substances, and data about its toxicity, safety hazards, and environmental impact is limited.

Check Digit Verification of cas no

The CAS Registry Mumber 885279-11-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 885279-11:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*9)+(2*1)+(1*1)=218
218 % 10 = 8
So 885279-11-8 is a valid CAS Registry Number.

885279-11-8SDS

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 2-(2-methoxyphenyl)-1,3-thiazole-4-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:885279-11-8 SDS

885279-11-8Downstream Products

885279-11-8Relevant articles and documents

The photoredox-catalyzed hydrosulfamoylation of styrenes and its application in the novel synthesis of naratriptan

Zhang, Mingjun,Chen, Miaomiao,Ding, Xin,Kang, Jin,Gao, Yongyue,He, Xingxing,Wang, Ziwen,Lu, Aidang,Wang, Qingmin

supporting information, p. 9140 - 9143 (2021/09/14)

The hydrosulfamoylation of diverse aryl olefins provides facile access to alkylsulfonamides. Here we report a novel protocol utilizing radical-mediated addition and a thiol-assisted strategy to achieve the hydrosulfamoylation of diverse styrenes in modest to excellent yields under mild and economic reaction conditions. The methodology was found to provide an efficient and convenient approach for the synthesis of the anti-migraine drug naratriptan and it also can be used for the late-stage functionalization of natural products or medicines.

Synthesis and biological properties of thiazole-analogues of pyochelin, a siderophore of Pseudomonas aeruginosa

No?l, Sabrina,Hoegy, Fran?oise,Rivault, Freddy,Rognan, Didier,Schalk, Isabelle J.,Mislin, Ga?tan L.A.

, p. 132 - 135 (2014/01/17)

Pyochelin is a siderophore common to all strains of Pseudomonas aeruginosa utilized by this Gram-negative bacterium to acquire iron(III). FptA is the outer membrane transporter responsible of ferric-pyochelin uptake in P. aeruginosa. We describe in this Letter the synthesis and the biological properties ( 55Fe uptake, binding to FptA) of several thiazole analogues of pyochelin. Among them we report in this Letter the two first pyochelin analogues able to bind FptA without promoting any iron uptake in P. aeruginosa.

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