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1,1,1-trichloro-3-nitropropan-2-ol, also known as Triclocarban, is a chlorinated aromatic compound primarily used as an antimicrobial agent in various personal care products, such as soaps, lotions, and cosmetics. It functions by disrupting the cell membrane of bacteria, thereby inhibiting their growth and reproduction. Triclocarban has been a subject of concern due to its potential endocrine-disrupting properties and environmental persistence, leading to its ban in certain countries and the development of alternative antimicrobial agents.

760-40-7

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760-40-7 Usage

Common uses

Biocidal and disinfectant applications

Chemical structure

Chlorinated nitro alcohol with three chlorine atoms and a nitro group attached to a propan-2-ol molecule

Industrial applications

Preservative in water-based systems, wood preservation, pharmaceuticals, and pesticides production

Antimicrobial properties

Effective against a wide range of microorganisms

Handling precautions

Hazardous to human health and the environment if not properly managed

Check Digit Verification of cas no

The CAS Registry Mumber 760-40-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 760-40:
(5*7)+(4*6)+(3*0)+(2*4)+(1*0)=67
67 % 10 = 7
So 760-40-7 is a valid CAS Registry Number.

760-40-7Relevant academic research and scientific papers

Highly regio- and stereoselective 1,3-dipolar cycloaddition of stabilised azomethine ylides to 3,3,3-trihalogeno-1-nitropropenes: Synthesis of trihalomethylated spiroindenepyrroli(zi)dines

Barkov, Alexey Yu.,Zimnitskiy, Nikolay S.,Kutyashev, Igor B.,Korotaev, Vladislav Yu.,Moshkin, Vladimir S.,Sosnovskikh, Vyacheslav Ya.

, p. 37 - 44 (2017/10/30)

Reactions of (E)-3,3,3-trihalogeno-1-nitropropenes with stabilised azomethine ylides derived from ninhydrin and indenoquinoxalinones on the one hand, and sarcosine and proline on the other, proceed regio- and diastereoselectively to give a number of trihalomethylated spiroindenepyrrolidines and spiroindenepyrrolizidines in good yields.

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