30478-88-7

Basic information

• Product Name: 2-NAPHTHALENOL, 3-BROMO-
• Synonyms: 2-NAPHTHALENOL, 3-BROMO-;3-broMonaphthalen-2-ol;3-Bromo-2-naphthol 99%
• CAS NO: 30478-88-7
• Molecular Formula: C₁₀H₇BrO
• Molecular Weight: 223.07
• Product Categories: Organic Building Blocks;Oxygen Compounds;Phenols;Building Blocks;C9 to C20+;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds
• Mol File: 30478-88-7.mol
• Article Data: 9

Chemical Properties

• Melting Point: 82 °C
• Boiling Point: 313.7°C at 760 mmHg
• Flash Point: 143.5°C
• Appearance: /
• Density: 1.614g/cm³
• Vapor Pressure: 0.000264mmHg at 25°C
• Refractive Index: 1.704
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 8.03±0.40(Predicted)
• CAS DataBase Reference: 2-NAPHTHALENOL, 3-BROMO-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-NAPHTHALENOL, 3-BROMO-(30478-88-7)
• EPA Substance Registry System: 2-NAPHTHALENOL, 3-BROMO-(30478-88-7)

Safety Data

• Hazard Codes: Xi
• Statements: 37/38-41
• Safety Statements: 26-39
• WGK Germany: 3
• Hazardous Substances Data: 30478-88-7(Hazardous Substances Data)

Usage

General Description

2-Naphthalenol, 3-bromo- is a chemical compound with the molecular formula C10H7BrO. It is a brominated derivative of naphthalenol, which is an aromatic alcohol. The compound is a white to light yellow solid with a melting point of 92-95°C. 2-Naphthalenol, 3-bromo- is primarily used in the synthesis of other organic compounds and as a reagent in chemical reactions. It is also used in research and development applications. The compound should be handled and stored with appropriate safety precautions, as it is considered hazardous if not properly managed.

InChI:InChI=1/C10H7BrO/c11-9-5-7-3-1-2-4-8(7)6-10(9)12/h1-6,12H

Upstream product

• 68251-77-4 2‐bromo‐3‐methoxynaphthalene 
• 30478-89-8 1,3-dibromonaphthalen-2-ol 
• 33670-69-8 3-bromo-2-hydroxy-naphthalene-1-diazonium-betaine 
• 93-18-5 2-ethoxynaphthalene 
• 50389-69-0 2-bromo-3-ethoxynaphthalene 
• 1449272-81-4 N,N-diethyl-O-((3-bromo)naphth-2-yl)-carbamate 
• 93-04-9 2-Methoxynaphthalene 
• 67291-63-8 2-amino-3-methoxynaphthalene 
• 13042-06-3 3-methoxy-[2]naphthoic acid amide 
• 135-19-3 β-naphthol 
• 858023-36-6 1,1,3,4,6,7-hexabromo-3,4,6,7-tetrahydro-1H-naphthalen-2-one 
• 54246-03-6 1,1-dibromo-1H-naphthalen-2-one 
• 7647-01-0 hydrogenchloride 
• 64-17-5 ethanol 

Downstream Products

• 1178513-70-6 (3-bromonaphthalen-2-yloxy)(tert-butyl)diphenylsilane 
• 1252059-90-7 (R)-2-[(3-bromonaphthalen-2-yloxy)methyl]-1-[(R)-1-phenylethyl]aziridine 
• 1351995-99-7 C₂₄H₁₉BrO 
• 1029917-00-7 3-bromo-2,2’-dihydroxy-1,1’-binaphthyl 
• 1424936-91-3 (1S,2S)-4-bromo-1,2-dihydro-2-nitro-1-phenylnaphtho[2,1-b]furan 
• 1556674-35-1 3-phenyl-2H-naphtho[2,3-e][1,4]dioxepin-5(3H)-one 
• 1556674-49-7 3-phenyl-2H-naphtho[2,3-e][1,4]dioxepin-5(3H)-one 
• 1611445-43-2 allyl 3-bromo-2-naphthyl ether 
• 52845-92-8 4-bromo-2-phenylnaphtho[1,2-d]oxazole 

Relevant articles and documents

Bi[naphtho[2,3-b]furanyl]: A versatile organic semiconductor with a furan-furan junction

[2,2′]Bi[naphtho[2,3-b]furanyl] was synthesized, characterized, and examined as an organic semiconductor for thin-film OFETs, bilayer OPVs, and organic light-emitting transistors (OLETs). In the devices, the material acted as a p-type semiconductor, showing moderately high mobility in OFETs, good photo conversion efficiency in OPVs, and blue-green emission in OLETs.

Enhancing the Antiaromaticity ofs-Indacene through Naphthothiophene Fusion

Addressing the instability of antiaromatic compounds often involves protection with bulky groups and/or fusion of aromatic rings, thus decreasing paratropicity. We report four naphthothiophene-fuseds-indacene isomers, one of which is more antiaromatic tha

Enantioselective Ni-Catalyzed Electrochemical Synthesis of Biaryl Atropisomers

A scalable enantioselective nickel-catalyzed electrochemical reductive homocoupling of aryl bromides has been developed, affording enantioenriched axially chiral biaryls in good yield under mild conditions using electricity as a reductant in an undivided cell. Common metal reductants such as Mn or Zn powder resulted in significantly lower yields in the absence of electric current under otherwise identical conditions, underscoring the enhanced reactivity provided by the combination of transition metal catalysis and electrochemistry.