What is the 1-BROMO-2,3,5,6-TETRAMETHYLBENZENE?

1-BROMO-2,3,5,6-TETRAMETHYLBENZENE is , while it's Molecular Formula is C10H13Br. Used in Research and Chemical Laboratories: 1-Bromo-2,3,5,6-tetramethylbenzene is used as a reagent, an intermediate, or as a building block in organic synthesis. Its bromine atom can be readily substituted by other functional groups, making it a valuable component in the preparation of various aroma compounds, polymers, dyestuffs, pharmaceuticals, and pesticides. Used in Organic Synthesis: 1-Bromo-2,3,5,6-tetramethylbenzene is used as a reagent for the synthesis of complex organic molecules. Its bromo functionality facilitates the substitution of the bromine atom with other functional groups, which is crucial for the development of new chemical entities. Used in the Preparation of Aroma Compounds: The chemical's bromine atom can be substituted to create a range of aroma compounds, making it useful in the fragrance industry. Used in the Production of Polymers: 1-Bromo-2,3,5,6-tetramethylbenzene can be incorporated into the structure of polymers, contributing to their properties and performance. Used in the Manufacture of Dyestuffs: 1-BROMO-2,3,5,6-TETRAMETHYLBENZENE's reactivity allows for the creation of various dyestuffs, which are essential in the textile and printing industries. Used in Pharmaceutical Development: 1-Bromo-2,3,5,6-tetramethylbenzene is used as a building block in the synthesis of pharmaceuticals, contributing to the development of new drugs. Used in Pesticide Formulation: 1-BROMO-2,3,5,6-TETRAMETHYLBENZENE's chemical properties make it a valuable component in the formulation of pesticides, enhancing their effectiveness in controlling pests.

What is the CAS number for 1-BROMO-2,3,5,6-TETRAMETHYLBENZENE?

The CAS number of 1-BROMO-2,3,5,6-TETRAMETHYLBENZENE is 1646-53-3.

What is 1-BROMO-2,3,5,6-TETRAMETHYLBENZENE (1646-53-3) used for?

1-Bromo-2,3,5,6-tetramethylbenzene, with the molecular formula C10H13Br, is a chemically synthesized compound that belongs to the organobromide class of compounds. It is an aromatic compound and appears as a clear liquid in its pure form. The presence of the bromine atom in its structure allows for versatile applications in various chemical processes.InChI:InChI=1/C10H13Br/c1-6-5-7(2)9(4)10(11)8(6)3/h5H,1-4H3

What is the 1-BROMO-2,3,5,6-TETRAMETHYLBENZENE?

1-BROMO-2,3,5,6-TETRAMETHYLBENZENE is , while it's Molecular Formula is C10H13Br. Used in Research and Chemical Laboratories: 1-Bromo-2,3,5,6-tetramethylbenzene is used as a reagent, an intermediate, or as a building block in organic synthesis. Its bromine atom can be readily substituted by other functional groups, making it a valuable component in the preparation of various aroma compounds, polymers, dyestuffs, pharmaceuticals, and pesticides. Used in Organic Synthesis: 1-Bromo-2,3,5,6-tetramethylbenzene is used as a reagent for the synthesis of complex organic molecules. Its bromo functionality facilitates the substitution of the bromine atom with other functional groups, which is crucial for the development of new chemical entities. Used in the Preparation of Aroma Compounds: The chemical's bromine atom can be substituted to create a range of aroma compounds, making it useful in the fragrance industry. Used in the Production of Polymers: 1-Bromo-2,3,5,6-tetramethylbenzene can be incorporated into the structure of polymers, contributing to their properties and performance. Used in the Manufacture of Dyestuffs: 1-BROMO-2,3,5,6-TETRAMETHYLBENZENE's reactivity allows for the creation of various dyestuffs, which are essential in the textile and printing industries. Used in Pharmaceutical Development: 1-Bromo-2,3,5,6-tetramethylbenzene is used as a building block in the synthesis of pharmaceuticals, contributing to the development of new drugs. Used in Pesticide Formulation: 1-BROMO-2,3,5,6-TETRAMETHYLBENZENE's chemical properties make it a valuable component in the formulation of pesticides, enhancing their effectiveness in controlling pests.

What is the CAS number for 1-BROMO-2,3,5,6-TETRAMETHYLBENZENE?

The CAS number of 1-BROMO-2,3,5,6-TETRAMETHYLBENZENE is 1646-53-3.

What is 1-BROMO-2,3,5,6-TETRAMETHYLBENZENE (1646-53-3) used for?

1-Bromo-2,3,5,6-tetramethylbenzene, with the molecular formula C10H13Br, is a chemically synthesized compound that belongs to the organobromide class of compounds. It is an aromatic compound and appears as a clear liquid in its pure form. The presence of the bromine atom in its structure allows for versatile applications in various chemical processes.InChI:InChI=1/C10H13Br/c1-6-5-7(2)9(4)10(11)8(6)3/h5H,1-4H3

1-BROMO-2,3,5,6-TETRAMETHYLBENZENE

High quality purity >99% 1-BROMO-2,3,5,6-TETRAMETHYLBENZENE 1646-53-3 for sale

Molecular Formula: C10H13Br
Molecular Weight: 213.117
Vapor Pressure: 0.0245mmHg at 25°C
Melting Point: 60-62 °C(lit.)
Refractive Index: 1.536
Boiling Point: 256.6 °C at 760 mmHg
Flash Point: 108.9 °C
PSA： 0.00000
Density: 1.248 g/cm³
LogP: 3.68270

1-BROMO-2,3,5,6-TETRAMETHYLBENZENE(Cas 1646-53-3) Usage

General Description

1-Bromo-2,3,5,6-tetramethylbenzene is a chemically synthesized compound that finds application primarily in research and chemical laboratories. It posses the molecular formula C10H13Br, and comes as a clear liquid in its pure form. This chemical is aromatic and belongs to the organobromide class of compounds which are organic compounds containing a bromine atom. It is used as a reagent, an intermediate or as a building block in organic synthesis due to its bromo functionality. The chemical's bromine atom can readily be substituted by other functional groups, thereby aiding in the preparation of various aroma compounds, polymers, dyestuffs, pharmaceuticals, and pesticides. It requires careful handling as it may cause eye and skin irritation and is harmful if inhaled or ingested. It is also not classified as a hazardous substance according to environmental regulations.

InChI:InChI=1/C10H13Br/c1-6-5-7(2)9(4)10(11)8(6)3/h5H,1-4H3

1646-53-3 Relevant articles

-

Newman,Lloyd

, p. 2672 (1952)

Introduction of an arylethynyl group onto an anthracene bisimide core for molecular design of new ?-conjugated compounds

Iwanaga, Tetsuo,Tanaka, Ryo,Toyota, Shinji

, p. 105 - 107 (2014/01/23)

Novel ethynylated anthracene bisimide (A...

Metal and H2O2 free aerobic oxidative aromatic halogenation with [RNH3+] [NO3-]/HX and [BMIM(SO3H)][NO3)x(X)y] (X = Br, Cl) as multifunctional ionic liquids

Prebil, Rok,Laali, Kenneth K.,Stavber, Stojan

supporting information, p. 2108 - 2111 (2013/06/05)

Novel multifunctional ionic liquids (ILs...

Influence of (2,3,4,5,6-pentamethyl/phenyl)phenyl scaffold: Stereoelectronic control of the persistence of o-quinonoid reactive intermediates of photochromic chromenes

Mandal, Susovan,Parida, Keshaba Nanda,Samanta, Subhas,Moorthy, Jarugu Narasimha

scheme or table, p. 7406 - 7414 (2011/11/06)

Regioisomeric photochromic chromenes 1Ch...

An efficient and regioselective monobromination of electron-rich aromatic compounds using catalytic hypervalent iodine(III) reagent

Zhou, Zhongshi,He, Xuehan

experimental part, p. 207 - 209 (2011/03/18)

An efficient and regioselective monobrom...

1646-53-3 Process route

: 95-93-2
1,2,4,5-tetramethylbenzene

: 1646-54-4
1,4-dibromodurene

: 1646-53-3
bromodurene

Conditions

Conditions	Yield
With hydrogen bromide; ethylammonium nitrate; In water; at 30 ℃; for 3h; Reagent/catalyst; regioselective reaction; Green chemistry;	61% 5%
With hydrogen bromide; dihydrogen peroxide; In water; at 20 ℃; for 24h; Darkness;	46% 25%

: 95-93-2
1,2,4,5-tetramethylbenzene

: 1646-53-3
bromodurene

Conditions

Conditions	Yield
With N-Bromosuccinimide; toluene-4-sulfonic acid; In methanol; for 21h; Product distribution; Mechanism; Ambient temperature; variation of conditions, other catalysts and reagents, without catalyst, + succinimide (NHS); other polyalkylbenzenes;	99%
With N-Bromosuccinimide; toluene-4-sulfonic acid; In methanol; for 21h; Ambient temperature;	99%
With N-Bromosuccinimide; In acetonitrile; at 0 - 20 ℃; Inert atmosphere;	92%
With sodium bismuthate; zinc dibromide; In acetic acid; at 20 ℃; for 0.5h;	82%
With PyHBrCl₂; In methanol; at 20 ℃; for 0.0833333h;	80%
With N-Bromosuccinimide; In acetonitrile; at 0 - 20 ℃; for 8h;	72%
With iodobenzene; toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; lithium bromide; In tetrahydrofuran; water; at 20 ℃; for 2h; regioselective reaction;	60%
With bromine; tetramethylammonium bromide; In liquid sulphur dioxide; at -23 ℃; Rate constant; Product distribution;
With bromine; acetic acid; at 0 ℃; Reinigung durch Destillation mit Wasser;
With chloroform; bromine; iodine;
With bromine; iodine; acetic acid;
With chloroform; bromine; iodine; at -10 - -5 ℃; Reinigung durch Destillation mit Wasser;
With tetrachloromethane; bromine; iodine; at 0 ℃;
With bromine; In water;
With N-Bromosuccinimide; In acetonitrile; at 20 ℃;