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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)-

2-chloro-4-morpholin-4-ylbenzaldehyde

O=Cc1ccc(cc1Cl)N1CCOCC1 Request for Quotation
Chemical Name: 2-chloro-4-morpholin-4-ylbenzaldehyde
CAS Number: 886501-36-6
Product Number: AG003GXM(AGN-PC-0LX08M)
Synonyms:
MDL No: MFCD06740104
Molecular Formula: C11H12ClNO2
Molecular Weight: 225.6715

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
225.672g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
225.056g/mol
Monoisotopic Mass:
225.056g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
219
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-4-morpholinobenzaldehyde is a versatile compound widely used in chemical synthesis as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it an essential intermediate in the production of a wide range of organic compounds.One of the main applications of 2-Chloro-4-morpholinobenzaldehyde is in the synthesis of heterocyclic compounds. By reacting this compound with different amines, alcohols, or other nucleophiles, chemists can access a variety of substituted morpholinobenzaldehydes and related structures. These products can serve as precursors for more complex molecules, including drugs, pesticides, and dyes.Additionally, 2-Chloro-4-morpholinobenzaldehyde can be utilized in the preparation of cross-coupling reagents and catalysts. Its chloro group can undergo various substitution reactions, enabling the introduction of different functional groups for modification or further elaboration. This compound plays a crucial role in designing and constructing novel organic molecules with desired properties.In summary, the significance of 2-Chloro-4-morpholinobenzaldehyde lies in its ability to serve as a valuable building block for the synthesis of diverse chemical compounds. Its reactivity and versatility make it a key component in the toolbox of synthetic chemists seeking to create innovative materials and products for various applications.