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2-Bromobenzaldehyde

  • Product Name: 2-Bromobenzaldehyde
  • CasNo: 6630-33-7
  • Purity:
  • Appearance: clear yellow liquid after melting

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CasNo: 6630-33-7

Molecular Formula: C7H5BrO

Appearance: clear yellow liquid after melting

99% Purity Commercial production 2-Bromobenzaldehyde 6630-33-7 with Cheapest Price

  • Molecular Formula:C7H5BrO
  • Molecular Weight:185.02
  • Appearance/Colour:clear yellow liquid after melting 
  • Vapor Pressure:5.27E-11mmHg at 25°C 
  • Melting Point:21-22 °C 
  • Refractive Index:n20/D 1.595(lit.)  
  • Boiling Point:230.8 °C at 760 mmHg 
  • Flash Point:96.2 °C 
  • PSA:17.07000 
  • Density:1.58 g/cm3 
  • LogP:2.26160 

2-Bromobenzaldehyde(Cas 6630-33-7) Usage

Chemical Description

2-bromobenzaldehyde is an organic compound with a molecular formula C7H5BrO.

InChI:InChI=1/C17H15NO4S2/c1-20-12-5-6-14(21-2)11(8-12)9-15-16(19)18(17(23)24-15)10-13-4-3-7-22-13/h3-9H,10H2,1-2H3/b15-9+

6630-33-7 Relevant articles

Rhodium-Catalyzed Asymmetric Allenylation of Sulfonylimines and Application to the Stereospecific Allylic Allenylation

Sieber, Joshua D.,Angeles-Dunham, Veronica V.,Chennamadhavuni, Divya,Fandrick, Daniel R.,Haddad, Nizar,Grinberg, Nelu,Kurouski, Dimitry,Lee, Heewon,Song, Jinhua J.,Yee, Nathan K.,Mattson, Anita E.,Senanayake, Chris H.

, p. 3062 - 3068 (2016)

The rhodium-catalyzed asymmetric allenyl...

Nickel(II)-Catalyzed Selective (E)-Olefination of Methyl Heteroarenes Using Benzyl Alcohols via Acceptorless Dehydrogenative Coupling Reaction

Balamurugan, Gunasekaran,Ramesh, Rengan

, (2021/11/30)

An efficient catalytic protocol for the ...

METHOD FOR OXIDATIVE CLEAVAGE OF COMPOUNDS WITH UNSATURATED DOUBLE BOND

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Paragraph 0071; 0077, (2021/07/10)

A method for oxidative cleavage of a com...

METHOD FOR OXIDATIVE CLEAVAGE OF COMPOUNDS WITH UNSATURATED DOUBLE BOND

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Paragraph 0053-0054; 0062-0063, (2021/03/19)

A method for oxidative cleavage of a com...

New method for promoting photosensitive oxidation to remove 1, 2-mercaptoethanol acetal protecting group by utilizing visible light irradiation

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Paragraph 0014-0016, (2021/01/30)

The invention discloses a new method for...

6630-33-7 Process route

methanol
67-56-1

methanol

o-bromobenzyl alcohol
18982-54-2

o-bromobenzyl alcohol

2-bromobenzoic acid methyl ester
610-94-6

2-bromobenzoic acid methyl ester

ortho-bromobenzaldehyde
6630-33-7

ortho-bromobenzaldehyde

Conditions
Conditions Yield
With tert.-butylhydroperoxide; potassium iodide; In water; at 65 ℃; for 24h;
2-bromobenzylamine
3959-05-5

2-bromobenzylamine

o-cyanobromobenzene
2042-37-7

o-cyanobromobenzene

ortho-bromobenzaldehyde
6630-33-7

ortho-bromobenzaldehyde

Conditions
Conditions Yield
With iodine; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In dimethyl sulfoxide; at 65 ℃; for 1.5h;
68%
6 %Chromat.

6630-33-7 Upstream products

  • 95-46-5
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    2-methylphenyl bromide

  • 29418-67-5
    29418-67-5

    2-bromobenzohydrazide

  • 2042-37-7
    2042-37-7

    o-cyanobromobenzene

  • 18982-54-2
    18982-54-2

    o-bromobenzyl alcohol

6630-33-7 Downstream products

  • 7345-79-1
    7345-79-1

    2-bromocinnamic acid

  • 108062-08-4
    108062-08-4

    (Z)-3-(2-bromophenyl)-2-phenylacrylonitrile

  • 55370-65-5
    55370-65-5

    (E)-3-(2-bromophenyl)-1-(2'-hydroxyphenyl)prop-2-en-1-one

  • 108791-79-3
    108791-79-3

    N-(2-bromobenzylidene)-2-hydroxyethylamine

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