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(5-NITRO-2-FURYL)METHYL AMINOMETHANIMIDOTHIOATE HYDROBROMIDE, a chemical compound with the molecular formula C7H9BrN4O3S, is a potent hydrobromide salt of the nitrofuryl derivative. It is characterized by its ability to act as an antimicrobial agent, making it a valuable component in pharmaceuticals and veterinary medicines.

82118-18-1

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82118-18-1 Usage

Uses

Used in Pharmaceutical Industry:
(5-NITRO-2-FURYL)METHYL AMINOMETHANIMIDOTHIOATE HYDROBROMIDE is used as an antimicrobial agent for treating bacterial infections in humans. It functions by disrupting the synthesis of DNA and RNA in the target microorganisms, which inhibits their growth and reproduction, thereby helping to clear the infection.
Used in Veterinary Medicine:
In the veterinary medicine industry, (5-NITRO-2-FURYL)METHYL AMINOMETHANIMIDOTHIOATE HYDROBROMIDE serves a similar purpose, being utilized as an antimicrobial agent to treat bacterial infections in animals. Its effectiveness in targeting and inhibiting the growth of microorganisms makes it a crucial component in maintaining animal health and preventing the spread of infections.

Check Digit Verification of cas no

The CAS Registry Mumber 82118-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,1 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82118-18:
(7*8)+(6*2)+(5*1)+(4*1)+(3*8)+(2*1)+(1*8)=111
111 % 10 = 1
So 82118-18-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N3O3S.BrH/c7-6(8)13-3-4-1-2-5(12-4)9(10)11;/h1-2H,3H2,(H3,7,8);1H

82118-18-1SDS

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 (5-nitrofuran-2-yl)methyl carbamimidothioate,hydrobromide

1.2 Other means of identification

Product number -
Other names (5-Nitrofuran-2-yl)methyl carbamimidothioate hydrobromide

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:82118-18-1 SDS

82118-18-1Relevant academic research and scientific papers

SYNTHESIS OF 5-(5-R-2-FURYL)THIAZOLE DERIVATIVES BY THE REACTION OF 2-(5-R-FURFURYL)THIURONIUM SALTS WITH ACETIC ANHYDRIDE

Usova, E. B.,Krapivin, G. D.,Kul'nevich, V. G.

, p. 477 - 482 (1990)

2-Acetamide-4-methyl-5-(5-R-2-furyl)thiazoles were obtained by the reaction of 2-(5-R-furfuryl)thiuronium salts with acetic anhydride.The reaction intermediates - 2-(5-R-furfuryl)-1,3-diacetylthioureas - were isolated and characterized.

Novel seleno- and thio-urea derivatives with potent in vitro activities against several cancer cell lines

Alcolea, Verónica,Plano, Daniel,Karelia, Deepkamal N.,Palop, Juan Antonio,Amin, Shantu,Sanmartín, Carmen,Sharma, Arun K.

, p. 134 - 144 (2016/03/01)

A series of novel selenourea derivatives and corresponding thiourea analogs were synthesized and tested against a panel of six human cancer cell lines: melanoma (1205Lu), lung carcinoma (A549), prostatic carcinoma (DU145), colorectal carcinoma (HCT116), p

Synthesis and antimicrobial and nitric oxide synthase inhibitory activities of novel isothiourea derivatives

Kazimierczuk, Zygmunt,Chalimoniuk, Malgorzata,Laudy, Agnieszka Ewa,Moo-Puc, Rosa,Cedillo-Rivera, Roberto,Starosciak, Bohdan Jerzy,Chrapusta, Stanislaw J.

experimental part, p. 821 - 830 (2012/01/05)

The reaction of substituted benzylhalides, or of halomethyl derivatives of thiophene or furane, with thiourea or its derivatives yielded the respective isothioureas as hydrohalide salts. The products (a total of 17, including 16 novel compounds) were test

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