4-Bromonaphthalen-1-ol

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Names

[ CAS No. ]:
571-57-3

[ Name ]:
4-Bromonaphthalen-1-ol

[Synonym ]:
4-bromo-1-hydroxynaphthalene
1-Naphthalenol,4-bromo
4-Bromo-1-naphthol
1-hydroxy-4-bromonaphthalene
4-bromo-1-naphthalenol
4-bromo-naphthalen-1-ol
4-bromonaphthalen-1-ol
1-Bromo-4-hydroxynaphthalene
1-Naphthalenol, 4-bromo-
4-bromonaphthol
4-BROMO-L-NAPHTHOL

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
346.4±15.0 °C at 760 mmHg

[ Melting Point ]:
128-133°C

[ Molecular Formula ]:
C10H7BrO

[ Molecular Weight ]:
223.066

[ Flash Point ]:
163.3±20.4 °C

[ Exact Mass ]:
221.968018

[ PSA ]:
20.23000

[ LogP ]:
3.72

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.705

[ Storage condition ]:
2-8°C

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H302 + H312-H315-H318-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2908199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 1-Naphthalenol
  • Dioxybis(trimethylsilane)
  • 1,4-Dibromonaphthalene
  • Naphthalene
  • benzo-4-bromo-2,5-cyclohexadienone
  • 1-Bromo-4-methoxynaphthalene
  • 1-Naphthalenecarboxylicacid, 4-hydroxy-
  • 2-Bromo-2-methylpropane

DownStream

  • 2,4-Dibromo-1-naphthol
  • 1-Bromo-4-methoxynaphthalene
  • 3,4-Dihydro-2H-pyran
  • Naphthalene, 1-bromo-4-(phenylmethoxy)-
  • 1-bromo-4-ethoxynaphthalene
  • 1-Naphthalenecarboxylicacid, 4-hydroxy-
  • 4-bromo-2-nitronaphthalen-1-ol
  • 1-(4-bromo-1-hydroxynaphthalen-2-yl)ethanone

Customs

[ HS Code ]: 2908199090

[ Summary ]:
HS: 2908199090. derivatives of polyphenols or phenol-alcohols containing only halogen substituents and their salts. VAT:17.0%. tax rebate rate:9.0%. supervision conditions:None. MFN tariff:5.5%. general tariff:30.0%

Articles

Enantioselective synthesis of (+)-estrone exploiting a hydrogen bond-promoted Diels-Alder reaction.

J. Org. Chem. 75 , 2718-2721, (2010)

Starting from Dane's diene and methylcyclopentenedione, (+)-estrone is synthesized along the Quinkert-Dane route in 24% total yield. The key step is an enantioselective Diels-Alder reaction promoted b...


More Articles

Related Compounds

  • (4-bromonaphthalen-1-yl)methanol
  • (4-bromonaphthalen-1-yl)-[2-(naphthalen-1-ylmethyl)phenyl]methanone
  • 7-bromonaphthalen-1-ol
  • 3,4-dibenzyl-2-bromonaphthalen-1-ol
  • 3-Bromo-1-hydroxynaphthalene
  • 5-(4-bromonaphthalen-1-yl)oxy-6-chloro-2-methylsulfanyl-1H-benzimidazole
  • 2-[3-(1,2-Dihydro-2-methyl-1-oxopyrrolo[1,2-a]pyrazin-3-yl)propyl]-1H-isoindole-1,3(2H)-dione
  • I+/--D-Glucofuranose, 3-O-methyl-1,2-O-(1-methylethylidene)-, cyclic carbonate
  • 2,3-Dihydro-6-methyl-5-(4-methylbenzoyl)-1H-pyrrolizine-1-carboxylic acid
  • Ethyl 5,7-dimethylimidazo[1,2-a]pyridine-2-carboxylate
  • Carbamic acid, [2-[(2-bromo-4-chlorophenyl)methylamino]-2-oxoethyl]-, phenylmethyl ester
  • 1-(2-Chlorophenyl)-4-{5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-yl}piperazine
  • N-Formyl-L-tyrosine propyl ester
  • (E)-3-(3-Acetoxy-4-methoxyphenyl)acrylic acid
  • (2S)-2-acetamido-3-(4-methoxyphenyl)-2-methylpropanoic acid
  • 3-(Trimethylsilyl)-4-pentenoic acid ethyl ester
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