1. Home
  2. Benzaldehyde, 2-amino-5-chloro-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzaldehyde, 2-amino-5-chloro-

O=Cc1cc(Cl)ccc1N Request for Quotation
Chemical Name: Benzaldehyde, 2-amino-5-chloro-
CAS Number: 20028-53-9
Product Number: AG002CNB(AGN-PC-0KKVRP)
Synonyms:
MDL No:
Molecular Formula: C7H6ClNO
Molecular Weight: 155.5816

Identification/Properties

Computed Properties
Molecular Weight:
155.581g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
155.014g/mol
Monoisotopic Mass:
155.014g/mol
Topological Polar Surface Area:
43.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
129
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Amino-5-chlorobenzaldehyde is a versatile compound widely used in chemical synthesis for its unique properties and capabilities. In organic chemistry, it serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its ability to undergo various reactions makes it a valuable building block in the synthesis of complex organic molecules.One of the primary applications of 2-Amino-5-chlorobenzaldehyde is in the synthesis of heterocyclic compounds, such as imidazoles and benzimidazoles, which have important biological activities. By reacting with different reagents and catalysts, this compound can be transformed into a variety of substituted derivatives, each with its own distinct chemical properties and applications.Furthermore, 2-Amino-5-chlorobenzaldehyde can also be utilized in the preparation of dyes, pigments, and polymers. Its chemical structure allows for easy modification and functionalization, enabling chemists to tailor its properties for specific applications. Overall, this compound plays a crucial role in the field of chemical synthesis, facilitating the creation of diverse compounds with various industrial and scientific uses.