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22177-94-2

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22177-94-2 Usage

General Description

CHEMBRDG-BB 7404777 is a chemical compound with a molecular formula of C16H15NO2. It is a long-acting β2-adrenergic receptor agonist and is used as a bronchodilator in the treatment of asthma and chronic obstructive pulmonary disease. It works by relaxing the muscles in the airways, which helps to open up the airways and make it easier to breathe. Additionally, this compound has been found to have anti-inflammatory properties, making it useful in the management of airway diseases characterized by inflammation. However, it is important to note that CHEMBRDG-BB 7404777 should be used under the guidance of a healthcare professional and may have side effects and interactions with other medications.

Check Digit Verification of cas no

The CAS Registry Mumber 22177-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,7 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22177-94:
(7*2)+(6*2)+(5*1)+(4*7)+(3*7)+(2*9)+(1*4)=102
102 % 10 = 2
So 22177-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H8ClN3O/c7-5-3-6(8-1-2-11)10-4-9-5/h3-4,11H,1-2H2,(H,8,9,10)

22177-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(6-Chloro-4-pyrimidinyl)amino]-1-ethanol

1.2 Other means of identification

Product number -
Other names 2-[(6-chloropyrimidin-4-yl)amino]ethanol

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:22177-94-2 SDS

22177-94-2Downstream Products

22177-94-2Relevant articles and documents

Effect of substituent structure on pyrimidine electrophilic substitution

van der Westhuyzen, Christiaan W.,Rousseau, Amanda L.,Parkinson, Christopher J.

, p. 5394 - 5405 (2008/01/07)

In an investigation into the electrophilic nitrosation reactions of a series of 4,6-disubstituted pyrimidine derivatives, a subtle interplay between the electronic nature of the C-4 and C-6 substituents and reactivity was found where these were chloro-, mono- or disubstituted amino groups. Effects such as the presence of an aryl group or two alkyl groups on the amino moiety impede the progress of the reaction despite the presence of a second activating group.

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