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22177-99-7

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22177-99-7 Usage

Uses

4-(6-chloro-2-methylpyrimidin-4-yl)morpholine is a useful research chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 22177-99-7 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 22177-99:
(7*2)+(6*2)+(5*1)+(4*7)+(3*7)+(2*9)+(1*9)=107
107 % 10 = 7
So 22177-99-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H12ClN3O/c1-7-11-8(10)6-9(12-7)13-2-4-14-5-3-13/h6H,2-5H2,1H3

22177-99-7SDS

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 4-(6-Chloro-2-methyl-4-pyrimidinyl)morpholine

1.2 Other means of identification

Product number -
Other names 4-(6-CHLORO-2-METHYLPYRIMIDIN-4-YL)MORPHOLINE

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:22177-99-7 SDS

22177-99-7Downstream Products

22177-99-7Relevant articles and documents

Novel Pyrimidine- And Triazine-Hepcidine Antagonists

-

, (2015/09/30)

The present invention relates to new hepcidin antagonists, pharmaceutical compositions containing them and the use thereof as a drug, in particular for the treatment of iron metabolism disorders such as, in particular, iron deficiency diseases and anaemia, in particular anaemia associated with chronic inflammatory disease (ACD: anaemia of chronic disease and AI: anaemia of inflammation).

Pyrimidines substituted by nitrogen-containing heterocyclic rings as intermediates

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, (2008/06/13)

1,2,4-Triazolo[4,3-c]pyrimidines substituted at the 5 or 7 position through a nitrogen atom which is part of a heterocyclic ring have been found to have potent bronchodilator activity and to be useful synthetic intermediates in the preparation of 1,2,4-triazolo[1,5-c]pyrimidines. Methods for inducing bronchodilation, pharmaceutical compositions, and synthetic processes and intermediates are also described.

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