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77199-09-8

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77199-09-8 Usage

General Description

5-bromo-2-pyridinecarboxylic acid ethyl ester is a chemical compound with the molecular formula C8H8BrNO2. It is a brominated derivative of 2-pyridinecarboxylic acid ethyl ester and belongs to the class of pyridinecarboxylic acids. 5-bromo-2-pyridinecarboxylic acid ethyl ester is commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. It has also been utilized as a reagent in the preparation of heterocyclic compounds and other organic intermediates. With its unique properties and versatile applications, 5-bromo-2-pyridinecarboxylic acid ethyl ester plays a crucial role in the field of chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 77199-09-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,9 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77199-09:
(7*7)+(6*7)+(5*1)+(4*9)+(3*9)+(2*0)+(1*9)=168
168 % 10 = 8
So 77199-09-8 is a valid CAS Registry Number.

77199-09-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 5-bromopicolinate

1.2 Other means of identification

Product number -
Other names 5-Bromo-pyridine-2-carboxylic acid ethyl ester

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:77199-09-8 SDS

77199-09-8Relevant articles and documents

Fusaric acid and analogues as Gram-negative bacterial quorum sensing inhibitors

Tung, Truong Thanh,Jakobsen, Tim Holm,Dao, Trong Tuan,Fuglsang, Anja Thoe,Givskov, Michael,Christensen, S?ren Br?gger,Nielsen, John

, p. 1011 - 1020 (2016/12/30)

Taking advantage of microwave-assisted synthesis, efficient and expedite procedures for preparation of a library of fusaric acid and 39 analogues are reported. The fusaric acid analogues were tested in cell-based screening assays for inhibition of the las and rhl quorum sensing system in Pseudomonas aeruginosa and the lux quorum sensing system in Vibrio fischeri. Eight of the 40 compounds in the library including fusaric acid inhibited lux quorum sensing and one compound inhibited activity of the las quorum sensing system. To our delight, none of the compounds showed growth inhibitory effects in the tested concentration ranges.

METALLOENZYME INHIBITOR COMPOUNDS

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Page/Page column 46; 47, (2014/04/03)

The instant invention describes compounds having metalloenzyme modulating activity, and methods of treating diseases, disorders or symptoms thereof mediated by such metalloenzymes. Living organisms have developed tightly regulated processes that specifica

FUSED HETEROCYCLIC RING DERIVATIVE AND USE THEREOF

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Page/Page column 115, (2012/07/14)

The present invention provides a fused heterocycle derivative having a strong Smo inhibitory activity, and use thereof. Specially, the present invention relates to a compound represented by the formula wherein each symbol is as defined in the specification, or salt thereof, and a medicament containing the compound or a prodrug thereof, which is an Smo inhibitor or an agent for the prophylaxis or treatment of cancer.

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