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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)-

Benzamide, 4-(hydroxymethyl)-N,N-dimethyl-

OCc1ccc(cc1)C(=O)N(C)C Request for Quotation
Chemical Name: Benzamide, 4-(hydroxymethyl)-N,N-dimethyl-
CAS Number: 60519-03-1
Product Number: AG00EDSO(AGN-PC-0JNMOR)
Synonyms:
MDL No:
Molecular Formula: C10H13NO2
Molecular Weight: 179.2157

Identification/Properties

Computed Properties
Molecular Weight:
179.219g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
179.095g/mol
Monoisotopic Mass:
179.095g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
172
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:
P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 4-(Hydroxymethyl)-N,N-dimethylbenzamide is a versatile chemical reagent utilized in various chemical synthesis applications. This compound serves as a valuable building block for the creation of complex organic molecules due to its unique structure and reactivity.In chemical synthesis, 4-(Hydroxymethyl)-N,N-dimethylbenzamide can be used as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its hydroxymethyl group can undergo various chemical transformations, such as oxidation, reduction, and substitution reactions, allowing for the introduction of different functional groups into the molecule. This versatility enables the synthesis of a wide range of compounds with diverse properties and applications.Additionally, the dimethylbenzamide moiety in this compound provides stability and structural rigidity, which are crucial for maintaining the integrity of the synthesized molecules. Furthermore, the presence of the dimethylamine group enhances the solubility and compatibility of the compound in different reaction conditions, making it a convenient reagent for use in various organic transformations.Overall, 4-(Hydroxymethyl)-N,N-dimethylbenzamide plays a crucial role in chemical synthesis by enabling the efficient construction of complex molecules with tailored properties and functionalities.