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105555-81-5

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105555-81-5 Usage

Classification

Synthetic antiprotozoal and antiviral agent
Belongs to the thiazolide class of compounds

Uses

Treatment of various parasitic and viral infections
Giardiasis
Cryptosporidiosis
Viral gastroenteritis
Potential treatment for influenza and hepatitis C

Mechanism of action

Interferes with the energy metabolism of parasites and viruses
Leading to their destruction

Side effects

Generally well-tolerated
Mild side effects such as nausea and headache (most common)

Importance

Versatile medication in the field of infectious diseases
Effective against a range of parasitic and viral infections
Potential for treating other diseases, increasing its value in medical treatments

Check Digit Verification of cas no

The CAS Registry Mumber 105555-81-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,5 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105555-81:
(8*1)+(7*0)+(6*5)+(5*5)+(4*5)+(3*5)+(2*8)+(1*1)=115
115 % 10 = 5
So 105555-81-5 is a valid CAS Registry Number.

105555-81-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-5-nitro-2-[(Z)-2-phenylprop-1-enyl]imidazole

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:105555-81-5 SDS

105555-81-5Downstream Products

105555-81-5Relevant articles and documents

REACTIONS SRN1 EN SERIE HETEROCYCLIQUE: II. REACTIVITE DU METHYL-1 CHLOROMETHYL-2 NITRO-5 IMIDAZOLE.

Crozet, Michel P.,Surzur, Jean-Marie,Vanelle, Patrice,Ghiglione, Claude,Maldonado, Jose

, p. 1023 - 1026 (1985)

1-Methyl-2-chloromethyl-5-nitroimidazole reacts with tertiary nitronate anions in excess to afford in high yields the previously unknown 1-methyl-5-nitro-imidazoles bearing a trisubstituted ethylenic double bond in the 2 position.These compounds are ascri

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