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3378-82-3

  • Product Name1-Bromo-2-naphthaldehyde
  • Molecular FormulaC11H7BrO
  • Molecular Weight235.08
  • Purity99%
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Product Details

Quick Details

  • CasNo: 3378-82-3
  • Molecular Formula: C11H7BrO
  • Purity: 99%

Buy high quality and low price 1-Bromo-2-naphthaldehyde 3378-82-3 now

  • Molecular Formula:C11H7BrO
  • Molecular Weight:235.08
  • Vapor Pressure:5.45E-05mmHg at 25°C 
  • Melting Point:118°C 
  • Refractive Index:1.7 
  • Boiling Point:347.3 °C at 760 mmHg 
  • Flash Point:119.8 °C 
  • PSA:17.07000 
  • Density:1.552 g/cm3 
  • LogP:3.41480 

1-Bromo-2-naphthaldehyde(Cas 3378-82-3) Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 46, p. 4617, 1981 DOI: 10.1021/jo00335a076

InChI:InChI=1/C11H7BrO/c12-11-9(7-13)6-5-8-3-1-2-4-10(8)11/h1-7H

3378-82-3 Relevant articles

A New Strategy for the Synthesis of Axially Chiral Biaryl Compounds

Rawal, Viresh H.,Florjancic, Alan S.,Singh, Surendra P.

, p. 8985 - 8988 (1994)

Axially chiral compounds can be synthesi...

Synthesis of Naphthocyclobutenes from α-Naphthyl Acrylates by Visible-Light Energy-Transfer Catalysis

Peez, Theodor,Schmalz, Veronika,Harms, Klaus,Koert, Ulrich

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Methyl (α-naphthyl) acrylates bearing an...

Rh-Catalyzed Formal [3+2] Cyclization for the Synthesis of 5-Aryl-2-(quinolin-2-yl)oxazoles and Its Applications in Metal Ions Probes

Zhou, Tongtong,He, Xinwei,Zuo, Youpeng,Wu, Yuhao,Hu, Wangcheng,Zhang, Shiwen,Duan, Jiahui,Shang, Yongjia

, p. 621 - 626 (2021/02/12)

A facile and efficient strategy for the ...

Tuning Flavin-Based Photocatalytic Systems for Application in the Mild Chemoselective Aerobic Oxidation of Benzylic Substrates

Tolba, Amal Hassan,Vávra, Franti?ek,Chudoba, Josef,Cibulka, Radek

supporting information, p. 1579 - 1585 (2019/12/24)

New flavin-based photocatalytic systems ...

NOVEL ORGANIC HETEROCYCLIC COMPOUND AND LIGHT-EMITTING DEVICE COMPRISING SAME

-

Paragraph 0163-0164, (2018/03/28)

The present invention relates to an orga...

3378-82-3 Process route

1-bromo-2-(bromomethyl)naphthalene
37763-43-2

1-bromo-2-(bromomethyl)naphthalene

1-bromo-2-naphthaldehyde
3378-82-3

1-bromo-2-naphthaldehyde

Conditions
Conditions Yield
With 2-nitropropane; sodium ethanolate; In ethanol; at 21 - 24 ℃; for 18h;
97%
With silver nitrate; In water; acetone;
80%
With 2-nitropropane; sodium ethanolate; In ethanol;
78%
With 4-methylmorpholine N-oxide; In acetonitrile; at 0 - 20 ℃; for 6h; Molecular sieve; Inert atmosphere;
73%
With 2-nitropropane; sodium ethanolate; In ethanol; for 6h; Heating;
62%
With ethanol; hexamethylenetetramine;
With hexamethylenetetramine; acetic acid;
With hydrogenchloride; N4(CH2)6; acetic acid; Yield given. Multistep reaction;
With 2-nitropropane; sodium ethanolate; In ethanol; at 20 ℃; for 65h;
Multi-step reaction with 2 steps
1: 95 percent / aq. CaCO3 / dioxane / 10 h / Heating
2: 79 percent / pyridinium chlorochromate (PCC)
With pyridinium chlorochromate; calcium carbonate; In 1,4-dioxane;
(1-bromo-2-naphthyl)methanol
76635-70-6

(1-bromo-2-naphthyl)methanol

1-bromo-2-naphthaldehyde
3378-82-3

1-bromo-2-naphthaldehyde

Conditions
Conditions Yield
With pyridinium chlorochromate; In dichloromethane; for 1h;
97%
With pyridinium chlorochromate; In dichloromethane; at 20 ℃; for 1.5h;
89%
With pyridinium chlorochromate;
79%

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