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ALPHA,3,5-TRIBROMO-2-HYDROXYTOLUENE, a brominated phenol, is a chemical compound known for its flame retardant properties. It is characterized by the presence of three bromine atoms and a hydroxyl group attached to a toluene molecule, which contributes to its effectiveness in reducing the flammability of materials.

4186-54-3

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4186-54-3 Usage

Uses

Used in Electronics Industry:
ALPHA,3,5-TRIBROMO-2-HYDROXYTOLUENE is used as a flame retardant additive in electronic devices to enhance fire safety and prevent potential hazards caused by overheating or electrical faults.
Used in Textile Industry:
In the textile industry, ALPHA,3,5-TRIBROMO-2-HYDROXYTOLUENE is utilized as a flame retardant in fabrics, providing additional protection against fire risks in various applications such as upholstery, carpets, and clothing.
Used in Plastics Industry:
ALPHA,3,5-TRIBROMO-2-HYDROXYTOLUENE is employed as a flame retardant in the production of various types of plastics, improving their fire resistance and reducing the risk of fire-related incidents.
However, due to concerns regarding the potential toxicity and environmental impact of ALPHA,3,5-TRIBROMO-2-HYDROXYTOLUENE, there is an ongoing search for safer alternatives to ALPHA,3,5-TRIBROMO-2-HYDROXYTOLUENE in flame retardant applications. The persistence of brominated compounds in the environment and their association with health risks have prompted efforts to develop more eco-friendly and less harmful flame retardants.

Check Digit Verification of cas no

The CAS Registry Mumber 4186-54-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,8 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4186-54:
(6*4)+(5*1)+(4*8)+(3*6)+(2*5)+(1*4)=93
93 % 10 = 3
So 4186-54-3 is a valid CAS Registry Number.

4186-54-3SDS

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 2,4-dibromo-6-(bromomethyl)phenol

1.2 Other means of identification

Product number -
Other names 2,4-Dibromo-6-bromomethylphenol

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:4186-54-3 SDS

4186-54-3Relevant academic research and scientific papers

Iron(iii)-salan complexes catalysed highly enantioselective fluorination and hydroxylation of β-keto esters and N-Boc oxindoles

Gu, Xin,Zhang, Yan,Xu, Zhen-Jiang,Che, Chi-Ming

supporting information, p. 7870 - 7873 (2014/07/08)

Chiral iron(iii)-salan complexes catalysed highly enantioselective α-fluorination and α-hydroxylation of β-keto esters and N-Boc oxindoles to give the corresponding products in high yields and good-to-excellent ee values under mild reaction conditions. This journal is the Partner Organisations 2014.

Exploitation of dinuclear salan aluminum complexes for versatile copolymerization of ε-caprolactone and l-lactide

Wang, Yuan,Ma, Haiyan

supporting information; experimental part, p. 6729 - 6731 (2012/08/14)

By combining the influence of excess alcohol, temperature and monomer-to-initiator ratios in the feed, dinuclear salan aluminum complexes LRAl2Me4 exhibited a high degree of control towards the copolymerization of l-LA and ε-CL, producing blocky, gradient, tapered and random copolymers.

Salalen titanium complexes in the highly isospecific polymerization of 1-hexene and propylene

Press, Konstantin,Cohen, Ad,Goldberg, Israel,Venditto, Vincenzo,Mazzeo, Mina,Kol, Moshe

supporting information; experimental part, p. 3529 - 3532 (2011/05/04)

All lined up: C1-symmetric octahedral titanium complexes (see structure, Ti dark gray, N blue, O red, I purple) whose labile positions reside in different electronic environments were designed using the readily available salalen ligands. With methylalumoxane as co-catalyst, highly active catalysts were obtained, which yielded high-molecular-weight polypropylene with ultra-high isotacticities (see 13C NMR spectrum) and melting transitions. Copyright

SALALEN LIGANDS AND ORGANOMETALLIC COMPLEXES

-

Page/Page column 49, (2012/01/06)

Use of homogeneous catalytic systems which include as a pre-catalyst a complex of a Group IV metal and a salalen ligand in the polymerization of alpha-olefins, is disclosed. The alpha-olefin polymers obtained are characterized by controlled levels of tacticity. Also disclosed are novel salalen ligands and novel complexes thereof with Group IV metals.

Electrophilic Substitution with Rearrangement. Part 9. Dienones derived from Brominations of o-, m-, and p-Cresol

Brittain, Judith M.,Mare, Peter B. D. de la,Newman, Paul A.

, p. 32 - 41 (2007/10/02)

Regiospecific protodebromination of ring-substituted bromophenols derived from 2-, 3-, or 4-methylphenol can be effected by heating them with aqueous hydrogen iodide; the synthetic scope of this reaction has been explored.These di- and poly-bromophenols can generally be converted by further bromination in aqueous acetic acid into dienones , which have now been shown to have the 4-bromo-2,5-dienone rather than the 2-bromo-3,5-dienone structure.The rearrangemens of these dienones to ring-substituted polybromophenols by treatment with sulfuric acid have been investigated; where more than one product is formed, the regioselectivity differs from that prevailing in the corresponding direct bromination of the phenol with liquid bromine.The alternative rearrangements of these dienones in aprotic solvents with and without illumination have been compared with results obtained by reaction of methylphenols with bromine under the same conditions.Characteristic differences between the behaviours of 2-, 3-, and 4-methyl-substituted compounds reflect the specific reactions available to the particular dienones.

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