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6-(2-Methoxypyrimidin-5-yl)-nicotinic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 216867-60-6 Structure
  • Basic information

    1. Product Name: 6-(2-Methoxypyrimidin-5-yl)-nicotinic acid
    2. Synonyms: 6-(Pyridin-4-yl)-nicotinic acid;6-(Pyrimidin-5-yl)-nicotinic acid;6-(2-Methoxypyrimidin-5-yl)-nicotinic acid;[2,4-Bipyridine]-5-carboxylic acid
    3. CAS NO:216867-60-6
    4. Molecular Formula: C11H9N3O3
    5. Molecular Weight: 200.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 216867-60-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-(2-Methoxypyrimidin-5-yl)-nicotinic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(2-Methoxypyrimidin-5-yl)-nicotinic acid(216867-60-6)
    11. EPA Substance Registry System: 6-(2-Methoxypyrimidin-5-yl)-nicotinic acid(216867-60-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 216867-60-6(Hazardous Substances Data)

216867-60-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 216867-60-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,8,6 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 216867-60:
(8*2)+(7*1)+(6*6)+(5*8)+(4*6)+(3*7)+(2*6)+(1*0)=156
156 % 10 = 6
So 216867-60-6 is a valid CAS Registry Number.

216867-60-6SDS

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 6-pyridin-4-ylpyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-(pyridin-4-yl)nicotinic acid

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:216867-60-6 SDS

216867-60-6Upstream product

216867-60-6Downstream Products

216867-60-6Relevant articles and documents

Three unprecedented open frameworks based on a pyridyl-carboxylate: Synthesis, structures and properties

Su, Shengqun,Chen, Wan,Song, Xuezhi,Zhu, Min,Qin, Chao,Song, Shuyan,Guo, Zhiyong,Wang, Song,Hao, Zhaoming,Li, Guanghua,Zhang, Hongjie

scheme or table, p. 1681 - 1686 (2012/05/20)

Three open frameworks, [Ni(pnta)2]·1.3DMF (1), [Zn 2(pnta)3(OH)]·2DMF (2), and [Cd(pnta) 2]·3.8DMF (3), were obtained by solvothermal reactions between 6-(pyridin-4-yl)nicotinic acid (Hpnta) and nickel(II), zinc(II) and cadmium(II) nitrate, respectively. Compound 1 is a chiral framework with a fourfold interpenetrated diamondoid network structure and two types of chiral channels. Compound 2 also possesses the fourfold interpenetrated adamantanoid architecture with helical rhombic nanotube-like channels, each of which has two sides of double-layer walls and two other sides of single-layer walls. Compound 3 is a rarely reported double-walled framework with bcu topology. The luminescent properties of compounds 2 and 3 have been studied in the solid state at room temperature.

Sulfonamide derivatives, their production and use

-

Referential example 27, (2010/11/29)

The present invention provides compounds which specifically inhibit FXa, which are effective when orally administered and which are useful as a safe medicine for the prevention or treatment of diseases caused by thrombus or infarction. Compounds of this invention are piperazinones of the formula: wherein R1is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group; the ring A is an optionally substituted divalent nitrogen-containing heterocyclic group, in addition to being substituted by the group of the formula: and the group of the formula: Y is an optionally substituted divalent hydrocarbon group or an optionally substituted divalent heterocyclic group; X is a direct bond or an optionally substituted alkylene chain; Z is (1) an amino group substituted with an optionally substituted hydrocarbon group, (2) an optionally substituted imino group or (3) an optionally substituted nitrogen-containing heterocyclic group; provided that when X is a direct bond and Z is an optionally substituted 6-membered nitrogen-containing aromatic heterocyclic group, Y is an optionally substituted divalent hydrocarbon group or an optionally substituted divalent unsaturated heterocyclic group; or a salt thereof.

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