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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)-

3-ALLYLSALICYLALDEHYDE

C=CCc1cccc(c1O)C=O Request for Quotation
Chemical Name: 3-ALLYLSALICYLALDEHYDE
CAS Number: 24019-66-7
Product Number: AG003ITL(AGN-PC-0WA7YV)
Synonyms:
MDL No:
Molecular Formula: C10H10O2
Molecular Weight: 162.1852

Identification/Properties

Properties
BP:
243.2°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Stability:
Air Sensitive
Refractive Index:
n20/D 1.5645
Solubility:
Soluble in chloroform.
Computed Properties
Molecular Weight:
162.188g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
162.068g/mol
Monoisotopic Mass:
162.068g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
165
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Allyl-2-hydroxybenzaldehyde, also known as cinnamyl salicylaldehyde, is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in the creation of various pharmaceuticals, fragrances, and agrochemicals due to its unique structural properties and reactivity.In chemical synthesis, 3-Allyl-2-hydroxybenzaldehyde acts as a crucial intermediate in the production of many important compounds. Its allyl group can undergo different reactions, such as allylation, to introduce additional functional groups into the molecule. The phenolic hydroxyl group can participate in nucleophilic substitution reactions, enabling the synthesis of diverse derivatives with enhanced biological activities.Furthermore, 3-Allyl-2-hydroxybenzaldehyde exhibits aromatic properties that allow it to participate in aromatic substitution reactions, leading to the formation of various substituted derivatives. These derivatives can have modified physicochemical properties, making them useful in a wide range of applications.Overall, the strategic placement of the allyl and hydroxyl groups in 3-Allyl-2-hydroxybenzaldehyde makes it a valuable tool in organic synthesis, enabling the creation of complex molecules with potential pharmacological, olfactory, or agricultural significance.