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Home > Encyclopedia > 6-Bromo-2-naphthalenol

6-Bromo-2-naphthalenol

6-Bromo-2-naphthalenol structure

6-Bromo-2-naphthalenol 

structure
  • CAS No:

    15231-91-1

  • Formula:

    C10H7BrO

  • Chemical Name:

    6-Bromo-2-naphthalenol

  • Synonyms:

    2-Naphthalenol,6-bromo-;2-Naphthol,6-bromo-;6-Bromo-2-naphthalenol;6-Bromo-β-naphthol;6-Bromo-2-naphthol;2-Bromo-6-hydroxynaphthalene;6-Bromo-2-hydroxynaphthalene;2-Hydroxy-6-bromonaphthalene;6-Hydroxy-2-bromonaphthalene;2-Bromo-6-naphthol;6-Bromo-2-naphthalinol;NSC 17563

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

off-white to beige powderChEBI: A member of the class of naphthols that is 2-naphthol carrying an additional bromo substituent at position 6.


6-bromo-2-naphthol is a member of the class of naphthols that is 2-naphthol carrying an additional bromo substituent at position 6. It is a member of naphthols and an organobromine compound. It derives from a 2-naphthol.

6-Bromo-2-naphthalenol Basic Attributes

223.07

223.07

1100270

239-279-0

87F10AHZ3O

17563

DTXSID5074551

29037990

Characteristics

20.2

3.4

Off-white to beige Powder

1.4412 (rough estimate)

127-128 °C

130°C (rough estimate)

167.8±20.4 °C

1.5700 (estimate)

Store at RT.

1.71E-05mmHg at 25°C

Safety Information

NONH for all modes of transport

3

36/37/38

26-36-37/39

QL3365000

Xi

Irritant

Stable at room temperature in closed containers under normal storage and handling conditions.

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 48 companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

6-bromo-2-naphthol

6-Bromo-2-naphthalenol Use and Manufacturing

Methods of Manufacturing

Derived from 2-naphthol through bromination and reduction. Add 2-naphthol and glacial acetic acid to the reaction pot, and then add the solution made of bromine and acetic acid. Add bromine, add water and heat to boiling, then add moss-like tin in batches when it is cooled to 100°C, and then boil it for 3 hours after addition, add 6-bromo-2-naphthol to the appropriate amount of cold water with stirring to precipitate, wash it with water, Filter and dry at 100°C to get crude product. After vacuum distillation, recrystallized to get the finished product.

Uses

6-Bromo-2-naphthol is a flavonoid molecule that shows steroid hormone activity and may be useful on anticancer therapy.

Computed Properties

Molecular Weight:223.07
XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Exact Mass:221.96803
Monoisotopic Mass:221.96803
Topological Polar Surface Area:20.2
Heavy Atom Count:12
Complexity:160
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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