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Thiazole, 4-ethynylis a chemical compound belonging to the thiazole family, characterized by the presence of a 4-ethynyl group. It is known for its various biological activities, such as antimicrobial, antifungal, and antiviral properties, making it a significant component in the development of new drugs and pesticides.

111600-89-6

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111600-89-6 Usage

Uses

Used in Pharmaceutical Industry:
Thiazole, 4-ethynylis used as a pharmaceutical compound for its antimicrobial, antifungal, and antiviral properties. The 4-ethynyl substitution enhances its pharmacological activities, making it a valuable addition to the development of new drugs.
Used in Agricultural Industry:
Thiazole, 4-ethynylis used as a pesticide due to its biological activities. The 4-ethynyl substitution improves its agricultural activities, contributing to the discovery of effective pesticides for crop protection.

Check Digit Verification of cas no

The CAS Registry Mumber 111600-89-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,6,0 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 111600-89:
(8*1)+(7*1)+(6*1)+(5*6)+(4*0)+(3*0)+(2*8)+(1*9)=76
76 % 10 = 6
So 111600-89-6 is a valid CAS Registry Number.

111600-89-6SDS

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 4-Ethynyl-1,3-thiazole

1.2 Other means of identification

Product number -
Other names 4-ethynyl-Thiazole

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:111600-89-6 SDS

111600-89-6Relevant articles and documents

HETEROCYCLIC COMPOUNDS AND USES THEREOF

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Paragraph 00655; 00659; 00709, (2015/04/22)

Compounds and pharmaceutical compositions that modulate kinase activity, including PI3 kinase activity, and compounds, pharmaceutical compositions, and methods of treatment of diseases and conditions associated with kinase activity, including PI3 kinase activity, are described herein.

HETEROCYCLIC COMPOUNDS FOR USE IN THE TREATMENT OF PI3K-GAMMA MEDIATED DISORDERS

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Paragraph 001311; 001315, (2015/11/10)

Compounds and pharmaceutical compositions that modulate kinase activity, including PI3 kinase activity, and compounds, pharmaceutical compositions, and methods of treatment of diseases and conditions associated with kinase activity, including PI3 kinase activity, are described herein.

p-Substituted Asymmetric Ureas and Medical Uses Thereof

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Paragraph 0253; 0255, (2015/09/28)

Disclosed are compounds, compositions and methods for the prevention and/or treatment of diseases which are pathophysiologically mediated by the ghrelin receptor. The compounds have the general Formula I: or pharmaceutically acceptable salts thereof.

2-CARBOXY THIOPHENE DERIVATIVES AS ANTI-VIRAL AGENTS

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Page/Page column 26-27, (2008/12/08)

Anti-viral agents of compounds of Formula (I) : wherein A, Rx, Ry, R2 and R3 are as defined in the specification, processes for their preparation and their use in HCV treatment are provided.

2-Thioethenyl substituted carbapenem derivatives

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Page/Page column 22, (2010/11/25)

[Objective] An objective of the present invention is to provide compounds that are effective against various resistant bacteria which cause current clinical problems, for example, pneumococci including penicillin resistant Streptococcus pneumoneae (PRSP),

INDOLE COMPOUNDS USEFUL AS IMPDH INHIBITORS

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Page column 42-43, (2010/02/04)

Compounds having the Formula (I), are effective as inhibitors of IMPDH enzyme, wherein R3 is alkyl, substituted alkyl, alkoxy, haloalkoxy, or halogen, preferably methoxy, ethoxy, or trifluoromethoxy; and R1, R2, R4, and R5 are as defined in the specificat

Palladium-Catalyzed Reactions of Terminal Acetylenes and Olefins with Halo-1,3-azoles

Sakamoto, Takao,Nagata, Hideo,Kondo, Yoshinori,Shiraiwa, Masafumi,Yamanaka, Hiroshi

, p. 823 - 828 (2007/10/02)

The palladium-catalyzed reactions of 4-bromo- and 5-bromothiazoles, as well as 4-bromo and 5-bromooxazoles with terminal acetylenes gave ethynyl derivatives in 43-89percent yields, whereas the reactions of 2-bromothiazoles and iodo-N-methylimidazoles affo

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