Login   |   Create New Account sales@aaronchem.com

Home > Products> 4542-77-2
4542-77-2

2,6-Bis(bromomethyl)naphthalene

Catalog#: AR0033PS  |   CAS#: 4542-77-2  |   MDL#: MFCD00228693  |   MF: C12H10Br2  |   MW: 314.0158

Packsize Purity Price Availability Quantity
100mg 97% $5.00 Global Stock Buy Now Add To Cart
250mg 97% $6.00 Global Stock Buy Now Add To Cart
1g 97% $23.00 Global Stock Buy Now Add To Cart
5g 97% $106.00 Global Stock Buy Now Add To Cart
10g 97% $200.00 Global Stock Buy Now Add To Cart
25g 97% $469.00 Global Stock Buy Now Add To Cart
  • Description
  • Application
  • Related Products
  • Featured Products
  • Safety Information
Catalog Number AR0033PS
Chemical Name 2,6-Bis(bromomethyl)naphthalene
CAS Number 4542-77-2
Molecular Formula C12H10Br2
Molecular Weight 314.0158
MDL Number MFCD00228693
SMILES BrCc1ccc2c(c1)ccc(c2)CBr

2,6-Bis(bromomethyl)naphthalene is a versatile compound widely used in chemical synthesis, particularly in the field of organic chemistry. This compound serves as a valuable building block for the preparation of various organic molecules through synthetic routes. Its unique structure with two bromomethyl groups attached to a naphthalene ring allows for selective functionalization and modification, making it a powerful tool for designing and creating new compounds.In chemical synthesis, 2,6-Bis(bromomethyl)naphthalene is commonly employed as a halogenated reagent for the introduction of bromomethyl groups into organic molecules. These bromomethyl groups can serve as key functional groups for further derivatization and diversification of the target compound. Additionally, the presence of two bromomethyl moieties in 2,6-Bis(bromomethyl)naphthalene offers the potential for symmetrical modification, enabling the synthesis of symmetrical molecules with enhanced properties and reactivity.Furthermore, the reactivity of the bromomethyl groups in 2,6-Bis(bromomethyl)naphthalene can be harnessed for various types of chemical transformations, such as nucleophilic substitution reactions, cross-coupling reactions, and metal-catalyzed transformations. This compound plays a crucial role in the development of novel organic molecules with tailored functionalities for applications in materials science, drug discovery, and chemical biology.Overall, the strategic use of 2,6-Bis(bromomethyl)naphthalene in chemical synthesis offers synthetic chemists a powerful tool for constructing complex organic structures and advancing the frontiers of molecular design and synthesis.
124405-67-0

2-Bromo-5-chloropyrimidine

124405-67-0

$5.00/100mg, $7.00/250mg, $10.00/500mg, $18.00/1g, $84.00/5g, $156.00/10g, $312.00/25g, $606.00/50g, $1,039.00/100g,

206989-61-9

1-Piperidinecarboxylic acid, 4-acetyl-, 1,1-dimethylethyl ester

206989-61-9

$4.00/1g, $7.00/5g, $12.00/10g, $30.00/25g, $109.00/100g, $268.00/250g, $529.00/500g,

85290-78-4

Ethyl 3-methyl-1H-pyrazole-4-carboxylate

85290-78-4

$4.00/1g, $4.00/250mg, $16.00/5g, $31.00/10g, $64.00/25g, $121.00/50g, $215.00/100g, $858.00/500g,

856859-49-9

4-Bromo-1H-pyrazolo[3,4-b]pyridine

856859-49-9

$7.00/50mg, $10.00/100mg, $12.00/250mg, $29.00/1g, $131.00/5g, $257.00/10g, $574.00/25g, $1,039.00/50g,

GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

Home| Products| Terms & Conditions| Ordering & Shipping| Company| Contact us

© 2019 Aaron Chemicals LLC. All Rights Reserved.