2-Amino-3,5-dibromobenzaldehyde

Names

[ Name ]:
2-Amino-3,5-dibromobenzaldehyde

[Synonym ]:
2-Amino-3,5-dibromobenzaldehyde
Ambroxol Hydrochloride Impurity E
EINECS 256-841-0
2-amino-3,5-dibromo-benzaldehyde
ZR BE DE FVH
3,5-Dibromoanthranilaldehyde
2-Amino-3,5-dibrom-benzaldehyd
3,5-dibromo-2-amino-benzaldehyde
Benzaldehyde, 2-amino-3,5-dibromo-
MFCD00671100
Ambroxol Impurity 2

Biological Activity

[Description]:

2-Amino-3,5-dibromobenzaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

[In Vitro]

50910-55-9|氨溴索杂质E对照品

Chemical & Physical Properties

[ Density]:
2.1±0.1 g/cm3

[ Boiling Point ]:
319.9±42.0 °C at 760 mmHg

[ Melting Point ]:
136-139 °C

[ Molecular Formula ]:
C₇H₅Br₂NO

[ Molecular Weight ]:
278.93

[ Flash Point ]:
147.3±27.9 °C

[ Exact Mass ]:
276.873779

[ PSA ]:
43.09000

[ LogP ]:
3.84

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.703

[ Storage condition ]:
-20?C Freezer

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H319

[ Precautionary Statements ]:
P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S37/39-S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2922399090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2922399090

[ Summary ]:
2922399090 other amino-aldehydes, amino-ketones and amino-quinones, other than those containing more than one kind of oxygen function; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

New tetradentate Schiff bases of 2-amino-3,5-dibromobenzaldehyde with aliphatic diamines and their metal complexes: synthesis, characterization and thermal stability.

Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 146 , 221-7, (2015)

The tetradentate Schiff base ligands (L(1)-L(4)), were synthesized by reaction between 2-amino-3,5-dibromobenzaldehyde and aliphatic diamines. Then, nickel and oxovanadium(IV) complexes of these ligan...

Regioselective facile one-pot Friedländer synthesis of sugar-based heterocyclic biomolecules.

Carbohydr. Res. 345(14) , 1988-97, (2010)

Regioselective facile one-pot synthesis of 16 different sugar-based quinoline, naphthyridine, and xanthone derivatives is reported. The compounds are characterized by NMR spectroscopy and elemental an...

Voltammetric behaviour of bromhexine and its determination in pharmaceuticals.

Talanta 73(5) , 913-9, (2007)

A complete electrochemical study and a novel electroanalytical procedure for bromhexine quantitation are described. Bromhexine in methanol/0.1molL(-1) Britton-Robinson buffer solution (2.5/97.5) shows...