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50290-51-2

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50290-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50290-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,2,9 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50290-51:
(7*5)+(6*0)+(5*2)+(4*9)+(3*0)+(2*5)+(1*1)=92
92 % 10 = 2
So 50290-51-2 is a valid CAS Registry Number.

50290-51-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1H-pyrimido[1,2-a]benzimidazol-4-one

1.2 Other means of identification

Product number -
Other names 2-methyl-1,5-dihydropyrimidino[1,2-a]benzimidazol-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:50290-51-2 SDS

50290-51-2Relevant articles and documents

Halogen-Containing 2-methylpyrimido[1,2-a]-benzimidazol-4(10H)-ones

Ulomskiy,El'Tsov,Borisov,Savateev,Voinkov,Fedotov,Rusinov

, p. 1005 - 1013 (2014)

We have synthesized a series of 3-halo-substituted pyrimidobenzimidazolones and studied the alkylation reaction of the obtained derivatives.

MRGX Receptor Antagonists

-

Paragraph 0300; 0310; 0311, (2021/05/07)

The invention relates to a method for preventing or treating a disease or disorder that is associated with the MrgX2 receptor. The invention also relates to MrgX2 antagonists and physiologically acceptable salts thereof. The invention also relates to pharmaceutical compositions and dosage forms comprising an MrgX2 antagonist.

Synthesis and characterization of some novel 2-(trifluoromethyl)pyrimido- [1,2-a]benzimidazoles and pyrimido[1,2-a]benzimidazol-2H-ones of biological interest

Zanatta, Nilo,Amaral, Simone S.,Esteves-Souza, Andressa,Echevarria, Aurea,Brondani, Patricia B.,Flores, Darlene C.,Bonacorso, Helio G.,Flores, Alex F. C.,Martins, Marcos A. P.

, p. 2305 - 2312 (2008/02/02)

The synthesis of some potentially active 2-(trifluoromethyl)pyrimido [1,2-a]benzimidazoles and pyrimido[1,2-a]benzimidazol-2(1H)-ones by the cyclization of 4-alkoxyvinyl trifluoro(chloro)methyl ketones with 2-aminobenzimidazole is described. The structure

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