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5851-47-8

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5851-47-8 Usage

Also known as

Ebastine

Classification

Second-generation, non-sedating antihistamine

Common uses

Treatment of allergic rhinitis and chronic idiopathic urticaria

Mechanism of action

Inhibits the effects of histamine released during an allergic reaction

Symptom relief

Itching, sneezing, and runny nose

Available forms

Tablets and oral solutions

Tolerability

Generally well-tolerated with few side effects

Importance

Valuable tool for managing allergy symptoms and providing relief for individuals with allergic conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 5851-47-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,5 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5851-47:
(6*5)+(5*8)+(4*5)+(3*1)+(2*4)+(1*7)=108
108 % 10 = 8
So 5851-47-8 is a valid CAS Registry Number.

5851-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-Pentanyl)-1H-benzimidazole

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:5851-47-8 SDS

5851-47-8Downstream Products

5851-47-8Relevant articles and documents

Photochemical Synthesis of Benzimidazoles from Diamines and Aldehydes

Skolia, Elpida,Apostolopoulou, Mary K.,Nikitas, Nikolaos F.,Kokotos, Christoforos G.

supporting information, p. 422 - 428 (2020/12/13)

An efficient, green, cheap, and metal-free photochemical protocol for the synthesis of benzimidazoles has been developed. 2,2-Dimethoxy-2-phenylacetophenone was employed as the photoinitiator and CFL lamps were used as the light source, leading to the cyc

Synthesis of 2-Substituted Benzimidazoles and 1,5-Disubstituted Benzodiazepines on Alumina and Zirconia Catalysts

Rekha,Hamza,Venugopal,Nagaraju

, p. 439 - 446 (2016/04/10)

In this study, alumina, zirconia, manganese oxide/alumina, and manganese oxide/zirconia have been investigated for their catalytic activity in the condensation reaction between o-phenylenediamine and an aldehyde or a ketone to synthesise 2-substituted benzimidazoles and 1,5-disubstituted benzodiazepines respectively. Surface area, surface acidity, and morphology of the catalysts have been analysed and correlated with their catalytic activity. The isolated yields of 2-substituted benzimidazoles and 1,5-disubstituted benzodiazepines are in the range of 30% to 95%. A good correlation between the amount of surface acid sites as well as the surface morphology of the catalysts and the catalytic activity has been observed. This method has been found to be simple and economical. The solid supports could be regenerated and reused without much loss in their activity. Further, the solid supports have been also found to be effective as general catalysts in the condensation of o-phenylenediamine with other substituted aldehydes and ketones.

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