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28890-99-5

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28890-99-5 Usage

General Description

BenziMidazole, also known as midazolobenziMidazole, is a chemical compound that belongs to the benzodiazepine class of drugs. It acts as a central nervous system depressant and is primarily used for its sedative, hypnotic, and anxiolytic effects. BenziMidazole is commonly prescribed for the treatment of anxiety, panic disorders, and insomnia. It works by enhancing the activity of a neurotransmitter called gamma-aminobutyric acid (GABA) in the brain, leading to a calming and relaxing effect. However, it may also cause side effects such as drowsiness, dizziness, and impaired coordination, and has the potential for abuse and dependence if used improperly. Therefore, it should only be used under the supervision of a healthcare professional and according to prescription guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 28890-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,9 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28890-99:
(7*2)+(6*8)+(5*8)+(4*9)+(3*0)+(2*9)+(1*9)=165
165 % 10 = 5
So 28890-99-5 is a valid CAS Registry Number.

28890-99-5SDS

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 benzimidazolo[1,2-a]benzimidazole

1.2 Other means of identification

Product number -
Other names 6H-benzimidazolo[1,2-a]benzimidazole

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:28890-99-5 SDS

28890-99-5Relevant articles and documents

RNA Hydrolysis by Heterocyclic Amidines and Guanidines: Parameters Affecting Reactivity

Danneberg, Friederike,Westemeier, Hauke,Horx, Philip,Zellmann, Felix,D?rr, Kathrin,Kalden, Elisabeth,Zeiger, Mirco,Akpinar, Abdullah,Berger, Robert,G?bel, Michael W.

, p. 6358 - 6366 (2021/10/06)

2-Aminobenzimidazole 10, although a weak catalyst in the monomeric state, is a successful building block for effective artificial ribonucleases. In an effort to identify new building blocks with improved catalytic potential, RNA cleavage by a variety of h

CONDENSED CYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

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Paragraph 0309; 0312; 0313, (2020/08/30)

A condensed cyclic compound represented by Formula 1 and an organic light-emitting device including the same: wherein, in Formulae 1, Y11 is a group represented by Formulae 2-1 to 2-3 and Y12 is a group represented by Formulae 3-1 to 3-5, 4-1, or 4-2 as described herein.

BENZIMIDAZOLO[1,2-A]BENZIMIDAZOLE CARRYING BENZIMIDAZOLO[1,2-A]BENZIMIDAZOLYL GROUPS, CARBAZOLYL GROUPS, BENZOFURANE GROUPS OR BENZOTHIOPHENE GROUPS FOR ORGANIC LIGHT EMITTING DIODES

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Page/Page column 290, (2017/08/01)

Benzimidazolo[1,2-a]benzimidazole carrying benzimidazolo[1,2-a]benzimidazolylyl groups, carbazolyl groups, dibenzofurane groups, dibenzothiophene groups, fluorenyl groups or dibenzosilolyl groups, an organic electronic device, comprising said benzimidazolo[1,2- a]benzimidazole carrying groups, a charge transport layer, charge blocking layer, charge/exciton blocking layer, or an emitting layer comprising said benzimidazolo[1,2-a]benzimidazole carrying groups, an apparatus selected from the group consisting of stationary visual display units; mobile visual display units; illumination units; keyboards; items of clothing; furniture; wallpaper, comprising said organic electronic device, or said charge transport layer, said charge/exciton blocking layer, or said emitting layer, the use of said benzimidazolo[1,2-a]benzimidazole carrying groups for organic electroluminescent devices, electrophotographic photoreceptors, photoelectric converters, organic solar cells, switching elements, organic light emitting field effect transistors, image sensors or dye lasers, and a process for the preparation of said benzimidazolo[1,2-a]benzimidazole carrying groups.

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