Name: Name:4-(Bromomethyl)pyridine hydrobromide
Brand: AABLOCKS
SKU: AA0033QG
Rating: 90 (10 reviews)

4-(Bromomethyl)pyridine hydrobromide is utilized as a key reagent in organic synthesis. It finds application in the preparation of various compounds, including nucleoside derivatives and benzoxazine derivatives. Specifically, it is involved in the synthesis of nucleoside analogs such as 3-(4-pyridylmethyl)-2′,3′-di-O-oleyl-5′-O-(4,4′-dimethoxytriphenylmethyl)uridine and 3-(4-pyridylmethyl)-3′-O-oleyl-5′-O-(4,4-dimethoxytriphenylmethyl)-thymidine. Additionally, it plays a crucial role in the synthesis of benzoxazine derivatives such as 2-morpholin-4-yl-7-(pyridin-4-ylmethoxy)-4H-1,3-benzoxazin-4-one and its analogs. Its reactivity and versatility make it an important precursor in the preparation of complex organic molecules with diverse applications in medicinal chemistry and materials science.

Catalog No.: AA0033QG

73870-24-3 | 4-(Bromomethyl)pyridine hydrobromide

Pack Size： 1g

Purity： 95%

in stock

$8.00 $6.00

Pack Size： 5g

Purity： 98%

in stock

$25.00 $17.00

Pack Size： 10g

Purity： 95%

in stock

$36.00 $26.00

Pack Size： 25g

Purity： 98%

in stock

$73.00 $51.00

Pack Size： 50g

Purity： 98%

in stock

$132.00 $92.00

Pack Size： 100g

Purity： 98%

in stock

$223.00 $156.00

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Technical Information

Catalog Number: AA0033QG

Chemical Name: 4-(Bromomethyl)pyridine hydrobromide

CAS Number: 73870-24-3

Molecular Formula: C6H7Br2N

Molecular Weight: 252.9345

MDL Number: MFCD01863545

SMILES: BrCc1ccncc1.Br

Properties

Form: Solid

MP: 189-192 °C(lit.)

Storage: Inert atmosphere;Room Temperature;

Complexity: 59.5

Covalently-Bonded Unit Count: 2

Defined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 9

Hydrogen Bond Acceptor Count: 1

Hydrogen Bond Donor Count: 1

Isotope Atom Count: 0

Rotatable Bond Count: 1

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

Application fold

4-(Bromomethyl)pyridine hydrobromide is utilized as a key reagent in organic synthesis. It finds application in the preparation of various compounds, including nucleoside derivatives and benzoxazine derivatives. Specifically, it is involved in the synthesis of nucleoside analogs such as 3-(4-pyridylmethyl)-2′,3′-di-O-oleyl-5′-O-(4,4′-dimethoxytriphenylmethyl)uridine and 3-(4-pyridylmethyl)-3′-O-oleyl-5′-O-(4,4-dimethoxytriphenylmethyl)-thymidine. Additionally, it plays a crucial role in the synthesis of benzoxazine derivatives such as 2-morpholin-4-yl-7-(pyridin-4-ylmethoxy)-4H-1,3-benzoxazin-4-one and its analogs. Its reactivity and versatility make it an important precursor in the preparation of complex organic molecules with diverse applications in medicinal chemistry and materials science.