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84227-79-2

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84227-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84227-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,2 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84227-79:
(7*8)+(6*4)+(5*2)+(4*2)+(3*7)+(2*7)+(1*9)=142
142 % 10 = 2
So 84227-79-2 is a valid CAS Registry Number.

84227-79-2SDS

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 1-Oxiranylmethyl-1H-benzoimidazole

1.2 Other means of identification

Product number -
Other names -

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:84227-79-2 SDS

84227-79-2Downstream Products

84227-79-2Relevant articles and documents

Heterocyclic chitosan oligosaccharide derivative and synthesis method thereof

-

Paragraph 0030; 0031; 0032; 0033; 0068, (2018/01/17)

The invention provides a heterocyclic chitosan oligosaccharide derivative and a synthesis method thereof. The method comprises the following concrete steps that (1) a heterocyclic compound is added into ethyl alcohol to be dissolved; after the solution is clear, hexadecyl trimethyl ammonium bromide and sodium hydroxide are added; after the stirring at normal temperature is performed, epoxy chloropropane is dropwise added; stirring is performed for 1.5 to 3h until white solids occur; when the white solids are not increased, reaction stops; a solid and liquid mixture is obtained; (2) chitosan oligosaccharide is added into distilled water to be dissolved; the solid and liquid mixture in the step (1) is added; constant-temperature stirring is performed for 3 to 5h at 60 to 80 DEG C; cooling is performed to room temperature, ethyl alcohol is added; still standing is performed for 12 to 15h; pressure reduction filtering is performed to obtain solids; the solids are washed twice by ethanol; drying is performed in a drying box. The prepared heterocyclic chitosan oligosaccharide derivative has good antibiotic activity and achieves a certain inhibiting effect on tobacco black shanks and corn stalk rot. The heterocyclic chitosan oligosaccharide derivative has good lipid solubility and water solubility, and can be easily absorbed by animals and plants; the activity is high.

Synthesis and Properties of N-2,3-Epoxypropyl Imidazole and Bisimidazole Derivatives

Korotkikh,Shvaika

, p. 1037 - 1046 (2007/10/03)

A number of mono- and bis-(2,3-epoxypropyl) derivatives of imidazoles, benzimidazoles, and bisbenzimidazoles, as well as their salts, were synthesized starting from corresponding azoles and 1-chloro-2,3-epoxypropane. On the basis of 1H NMR and IR spectral data, one of the y-protons in the oxirane ring is presumed to participate in intramolecular H-π interaction with aromatic rings of the azoles. The obtained compounds exhibit antitumor activity and luminescent properties and are potential hardeners and cohardeners for epoxy resins.

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