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Benzenemethanol, 2,4-dichloro-α-(trichloromethyl)-, also known as 2,4-dichloro-α-(trichloromethyl)benzenemethanol, is an organic compound with the chemical formula C7H5Cl5O. It is a derivative of benzyl alcohol, featuring two chlorine atoms at the 2nd and 4th positions on the benzene ring, and a trichloromethyl group (CCl3) attached to the α-carbon of the benzyl alcohol. Benzenemethanol, 2,4-dichloro-a-(trichloromethyl)- is characterized by its potential reactivity and may have applications in the synthesis of various organic compounds. Due to the presence of multiple chlorine atoms, it is important to handle this substance with care, as it may pose environmental and health risks.

6781-47-1

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6781-47-1 Usage

Commonly known as

Triclosan

Use

Antibacterial and antifungal agent in consumer products

Products

Soaps, toothpastes, body washes

Properties

Antimicrobial

Concerns

Potential impact on human health and environment

Linked to

Hormone disruption, antibiotic resistance, ecological harm

Restrictions

In some countries

Recommendation

Consider potential risks and seek alternative, safer options.

Check Digit Verification of cas no

The CAS Registry Mumber 6781-47-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,8 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6781-47:
(6*6)+(5*7)+(4*8)+(3*1)+(2*4)+(1*7)=121
121 % 10 = 1
So 6781-47-1 is a valid CAS Registry Number.

6781-47-1Relevant academic research and scientific papers

The Reaction of Polyhalogenomethanes with Aldehydes and with 1,3,5-Trinitrobenzene in the Presence of Tin(II) Salts: Evidence for the Formation of Trihalogenomethyl Anions

Atkins, Paul J.,Gold, Victor,Routledge, Paul J.

, p. 1563 - 1566 (2007/10/02)

The (previously reported) formation of 2,2,2-tribromoethanols by the reaction of aromatic aldehydes with tetrabromomethane in the presence of tin(II) fluoride in dimethyl sulphoxide solution also occurs when tin(II) chloride is used in place of the fluoride.Analogous reactions occur with certain other tetrahalogenomethanes, but not with trihalogenomethanes nor with fluorine-containing tetrahalogenomethanes.When the aldehyde is replaced by 1,3,5-trinitrobenzene, Meisenheimer adducts derived from trihalogenomethyl anions are formed.The trihalogenomethyl anions are thought to be a product of the two-electron reduction of tetrahalogenomethanes by tin (II).

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