552-89-6

  • Product Name:2-nitrobenzaldehyde
  • Molecular Formula:C7H5NO3
  • Purity:99%
  • Molecular Weight:151.122
Inquiry

Product Details

Buy High Quality Wholesale 2-nitrobenzaldehyde 552-89-6 with Safe Shipping

  • Molecular Formula:C7H5NO3
  • Molecular Weight:151.122
  • Appearance/Colour:Yellow crystalline powder or needles 
  • Vapor Pressure:0.0078mmHg at 25°C 
  • Melting Point:42-44 °C(lit.) 
  • Refractive Index:1.617 
  • Boiling Point:268.2 °C at 760 mmHg 
  • Flash Point:144 °C 
  • PSA:62.89000 
  • Density:1.338 g/cm3 
  • LogP:1.93050 

2-Nitrobenzaldehyde(Cas 552-89-6) Usage

Description

The 2-Nitrobenzyl group of 2-nitrobenzaldehyde is photolabile that can be cleaved when exposed to UV-light. 2-nitrobenzaldehydes are yellow or bright yellow needle-like crystals. It can volatilize with water vapor and has the fragrance of benzaldehyde. Soluble in ethanol, ether, benzene, slightly soluble in water, flash point>110℃, reacts violently with pyrrole.

Uses

2-Nitrobenzaldehyde is a benzaldhyde with a nitro group substituted in the ortho position. 2-Nitrobenzaldehyde is used in the preparation of dyes and colorants such as Indigo carmine. 2-Nitrobenzaldehyde gas been shown to be a useful photoremovable protecting group as well as in the preparation of more effective ones such as o-Nitrophenylethylene glycol.

InChI:InChI=1/C7H5NO3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-5H

552-89-6 Relevant articles

Synthesis of bimagnetic ionic liquid and application for selective aerobic oxidation of aromatic alcohols under mild conditions

Miao, Cheng-Xia,Wang, Jin-Quan,Yu, Bing,Cheng, Wei-Guo,Sun, Jian,Chanfreau, Sebastien,He, Liang-Nian,Zhang, Suo-Jiang

, p. 2697 - 2699 (2011)

The first bimagnetic ionic liquid based ...

Nitrolysis of 2,6,8,12-tetraacetyl-4,10-dibenzyl-2,4,6,8,10,12-hexaazatetracyclo[5.5.0.03,11.05,9]dodecane

Kalashnikov,Sysolyatin,Sakovich,Dubkov,Kulagina

, p. 531 - 536 (2017)

Nitrolysis of 2,6,8,12-tetraacetyl-4,10-...

Continuous flow nitration of benzaldehyde

Kulkarni, Amol A.,Kalyani, Vishwanath S.,Joshi, Ramesh A.,Joshi, Rohini R.

, p. 999 - 1002 (2009)

The nitration of benzaldehyde can be car...

Conversion of oximes into carbonyl compounds with thalium(III) nitrate supported onto HZSM-5 zeolite under microwave irradiation in solventless system

Heravi, Majid M.,Ghassemzadeh, Mitra

, p. 119 - 123 (2003)

Oximes are oxidatively deprotected by th...

Kinetics and Thermodynamics of Restricted Rotation of the Formyl Group in Nitrobenzaldehyde Anion Radicals

Branca, Mario,Gamba, Aldo,Barzaghi, Mario,Simonetta, Massimo

, p. 6506 - 6515 (1982)

The barrier to rotation about the carbon...

Oxidation of benzyl alcohols under mild heterogeneous conditions

Shirini,Zolfigol,Azadbar

, p. 1600 - 1602 (2001)

A combination of iodic acid with ammoniu...

Facile open air oxidation of benzylic alcohols in distilled water by in situ made copper(II) complexes

Ahmad, Jahir Uddin,R?is?nen, Minna T.,Kemell, Marianna,Heikkil?, Mikko J.,Leskel?, Markku,Repo, Timo

, p. 153 - 162 (2012)

A highly efficient, selective and green ...

Preparation method of o-nitrobenzaldehyde

-

, (2021/12/07)

The invention relates to the technical f...

Non-alkylator anti-glioblastoma agents induced cell cycle G2/M arrest and apoptosis: Design, in silico physicochemical and SAR studies of 2-aminoquinoline-3-carboxamides

Gu, Xiangyu,Liu, Jianwen,Ni, Xintong,Qi, Yingxue,Qian, Xuhong,Shao, Xusheng,Xu, Xiaoyong,Yuan, Pengtao

supporting information, (2021/09/22)

Malignant gliomas are the most common br...

The: In situ fabrication of ZIF-67 on titania-coated magnetic nanoparticles: A new platform for the immobilization of Pd(ii) with enhanced catalytic activity for organic transformations

Kaur, Manpreet,Paul, Satya,Sharma, Chandan,Sharma, Sukanya

, p. 20309 - 20322 (2021/11/22)

Considering the outstanding characterist...

Nitration of deactivated aromatic compounds via mechanochemical reaction

Wu, Jian-Wei,Zhang, Pu,Guo, Zhi-Xin

supporting information, (2021/05/05)

A variety of deactivated arenes were nit...

552-89-6 Process route

o-nitrobenzaldehyde diethylacetal
88356-11-0

o-nitrobenzaldehyde diethylacetal

ethyl 2-nitrobenzoate
610-34-4

ethyl 2-nitrobenzoate

2-ethoxymethyl-1-nitrobenzene
66424-93-9

2-ethoxymethyl-1-nitrobenzene

2-nitro-benzaldehyde
552-89-6

2-nitro-benzaldehyde

Conditions
Conditions Yield
aluminum oxide; In gas; at 350 ℃; Yield given;
 
aluminum oxide; In gas; at 200 ℃; Yield given;
 
bis-(α-bromo-2-nitro-benzyl)-ether

bis-(α-bromo-2-nitro-benzyl)-ether

hydrogen bromide
10035-10-6,12258-64-9

hydrogen bromide

2-nitro-benzaldehyde
552-89-6

2-nitro-benzaldehyde

Conditions
Conditions Yield
 
 

552-89-6 Upstream products

  • 91-22-5
    91-22-5

    quinoline

  • 99-65-0
    99-65-0

    meta-dinitrobenzene

  • 612-25-9
    612-25-9

    2-Nitrobenzyl alcohol

  • 497-19-8
    497-19-8

    sodium carbonate

552-89-6 Downstream products

  • 577-59-3
    577-59-3

    2-acetylnitrobenzene

  • 1969-72-8
    1969-72-8

    (2-nitrophenyl)acetone

  • 39830-70-1
    39830-70-1

    (+/-)-2-(2-nitrophenyl)oxirane

  • 124525-52-6
    124525-52-6

    2-methyl-3t-(2-nitro-phenyl)-acrylic acid

Relevant Products