CAS 571-57-3|4-Bromonaphthalen-1-ol

Introduction：Basic information about CAS 571-57-3|4-Bromonaphthalen-1-ol, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. Chemical & Physical Properties
3. Safety Information
4. Customs
5. Articles1
6. Synonyms

Common Name	4-Bromonaphthalen-1-ol
CAS Number	571-57-3	Molecular Weight	223.066
Density	1.6±0.1 g/cm3	Boiling Point	346.4±15.0 °C at 760 mmHg
Molecular Formula	C₁₀H₇BrO	Melting Point	128-133°C
MSDS	ChineseUSA	Flash Point	163.3±20.4 °C
Symbol	GHS05, GHS07	Signal Word	Danger

Names

Name	4-bromonaphthalen-1-ol
Synonym	More Synonyms

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
InChIKey	OUNQUWORSXHSJN-UHFFFAOYSA-N
SMILES	Oc1ccc(Br)c2ccccc12
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

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%

Articles1

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...

Synonyms

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

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