2-Amino-3,5-dibromobenzaldehyde CAS 50910-55-9

2-Amino-3,5-dibromobenzaldehyde CAS 50910-55-9

Identification

CAS Number

50910-55-9

Name

2 Amino 3 5 Dibromo Benzaldehyde

Synonyms

256-841-0 [EINECS]
2-Amino-3,5-dibrombenzaldehyd [German] [ACD/IUPAC Name]
2-Amino-3,5-dibromobenzaldehyde [ACD/IUPAC Name]
2-Amino-3,5-dibromobenzaldéhyde [French] [ACD/IUPAC Name]
3247660 [Beilstein]
50910-55-9 [RN]
Benzaldehyde, 2-amino-3,5-dibromo- [ACD/Index Name]
MFCD00671100 [MDL number]
ZR BE DE FVH [WLN]
2,2′-((1E,1’E)-hydrazine-1,2-diylidenebis(methanylylidene))diphenol
256-841-0MFCD00671100
2-Amino-3,5-dibrombenzolcarbaldehyd
2-Amino-3,5-DibromoBenzaldehyde (en)
3,5-Dibromoanthranilaldehyde
32644-15-8 [RN]
32659-49-7 [RN]
AC1LELSO
ACMC-209kqx
MFCD00137325 [MDL number]
MFCD00210112 [MDL number]
OR-0650
PubChem8245
S-2–bromobutyric acid
Salicylaldehyde azine
SBB063039

SMILES

c1c(cc(c(c1C=O)N)Br)Br

StdInChI

InChI=1S/C7H5Br2NO/c8-5-1-4(3-11)7(10)6(9)2-5/h1-3H,10H2

StdInChIKey

RCPAZWISSAVDEA-UHFFFAOYSA-N

Molecular Formula

C7H5Br2NO

Molecular Weight

278.929

EINECS

256-841-0

MDL Number

MFCD00671100

Properties

Appearance

Yellow Crystalline Powder

Structure

Structure of 2-Amino-3,5-dibromobenzaldehyde CAS 50910-55-9

Structure of 2-Amino-3,5-dibromobenzaldehyde CAS 50910-55-9

Melting Point

137~140°C

Safety Data

Symbol

exclamation-mark-jpgGHS07

Signal Word

Warning

Hazard statements

H319

Precautionary Statements

P264 – P280 – P305 + P351 + P338 – P337 + P313

WGK Germany

3

MSDS Download

Specifications and Other Information of Our

Identification Methods

HNMR, HPLC

Assay

99.91% min

Loss on Drying

≤ 0.1%

Residue on Ignition

≤ 0.1%

Any Other Individual Impurity

≤ 0.1%

Total Impurities

≤ 0.1%

Shelf Life

2 years

Storage

Keep material sealed and store in cool, dry place, away from sunlight and moisture.

Known Application

2-Amino-3-5 Dibromo Benzaldehyde can serve as an intermediate in organic synthesis. It can participate in various chemical reactions such as amination, electrophilic substitution, condensation reactions, etc., to construct the framework of complex organic molecules or synthesize target compounds.

This compound may be utilized in the synthesis of pharmaceutical intermediates or key structural units. Its chemical properties and functional groups can provide diversity and flexibility in the design and synthesis of drug molecules. And 2-Amino-3,5-dibromobenzaldehyde can find applications in analytical chemistry. It may be used as a colorimetric reagent, indicator, or ligand for the detection or analysis of specific compounds or ions.

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