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6622-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6622-92-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6622-92:
100 % 10 = 0
So 6622-92-0 is a valid CAS Registry Number.

6622-92-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A10960)  6-Hydroxy-2,4-dimethylpyrimidine, 99%   

  • 6622-92-0

  • 5g

  • 347.0CNY

  • Detail
  • Alfa Aesar

  • (A10960)  6-Hydroxy-2,4-dimethylpyrimidine, 99%   

  • 6622-92-0

  • 25g

  • 1194.0CNY

  • Detail
  • Aldrich

  • (D165158)  4-Hydroxy-2,6-dimethylpyrimidine  ≥99%

  • 6622-92-0

  • D165158-5G

  • 345.15CNY

  • Detail



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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017


1.1 GHS Product identifier


1.2 Other means of identification

Product number -
Other names 2,6-dimethyl-1H-pyrimidin-4-one

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:6622-92-0 SDS

6622-92-0Relevant articles and documents

Ultrasound-Promoted Synthesis of 4-Pyrimidinols and Their Tosyl Derivatives

Vidal, Matías,García-Arriagada, Macarena,Rezende, Marcos Caroli,Domínguez, Moisés

, p. 4246 - 4252 (2016/11/26)

Ultrasound irradiation promoted the cyclocondensation of β-keto esters and amidines in good to excellent yields to form sixteen highly substituted 4-pyrimidinols. Tosylation of these compounds, in another ultrasound-promoted conversion, formed 4-pyrimidyl tosylates in high yields. The use of the developed protocol as an alternative route to 4-arylpyrimidines was illustrated with three examples of the Suzuki-Miyaura cross-coupling of the prepared tosylates with phenylboronic acid.



Paragraph 00374; 00375, (2013/06/05)

Agents for modulating methyl modifying enzymes, compositions and uses thereof are provided herein



Page/Page column 159-160, (2012/04/23)

A cyclopropane compound represented by the following formula (A) or a pharmaceutically acceptable salt thereof has orexin receptor antagonism, and therefore has a potencial of usefulness for the treatment of sleep disorder for which orexin receptor antagonism is effective, for example, insomnia: wherein Q represents —CH— or a nitrogen atom, R1a and R1b each independently represent a C1-6 alkyl group and the like, R1c represents a hydrogen atom and the like, R2a, R2b, R2c and R2d each independently represent a hydrogen atom, a halogen atom, a C1-6 alkyl group and the like, R3a, R3b and R3c each independently represent a hydrogen atom, a halogen atom and the like, and R3d represents a hydrogen atom and the like.

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