183057-64-9

Basic information

• Product Name: 4-(HYDROXYMETHYL)BENZALDEHYDE DIMETHYL ACETAL
• Synonyms: 4-(HYDROXYMETHYL)BENZALDEHYDE DIMETHYL ACETAL;P-(DIMETHOXYMETHYL)BENZYL ALCOHOL;4-(HYDROXYMETHYL)BENZALDEHYDE DIMETHYL;4-(dimethoxymethyl)benzyl alcohol;4-(HYDROXYMETHYL)BENZALDEHYDE DIMETHYL ACETAL 98+%;(4-(Dimethoxymethyl)phenyl)methanol;p-Hydroxymethylbenzaldehyde dimethyl acetal;4-(Hydroxymethyl)benzaldehyde dimethyl acetal >=97.0% (GC)
• CAS NO: 183057-64-9
• Molecular Formula: C₁₀H₁₄O₃
• Molecular Weight: 182.22
• Mol File: 183057-64-9.mol

Chemical Properties

• Melting Point: 38-42 °C
• Boiling Point: 261℃
• Flash Point: 112℃
• Appearance: /
• Density: 1.097
• Vapor Pressure: 0.00611mmHg at 25°C
• Refractive Index: 1.518
• Storage Temp.: 2-8°C
• PKA: 14.32±0.10(Predicted)
• BRN: 2577568
• CAS DataBase Reference: 4-(HYDROXYMETHYL)BENZALDEHYDE DIMETHYL ACETAL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(HYDROXYMETHYL)BENZALDEHYDE DIMETHYL ACETAL(183057-64-9)
• EPA Substance Registry System: 4-(HYDROXYMETHYL)BENZALDEHYDE DIMETHYL ACETAL(183057-64-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• WGK Germany: 3
• F: 10
• Hazardous Substances Data: 183057-64-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
4-(HYDROXYMETHYL)BENZALDEHYDE DIMETHYL ACETAL is used as a synthetic intermediate for the development of pharmaceutical compounds. Its ability to react with other molecules and form new compounds makes it a valuable component in the creation of potential drugs and therapeutic agents.
Used in Chemical Synthesis:
In the field of chemical synthesis, 4-(HYDROXYMETHYL)BENZALDEHYDE DIMETHYL ACETAL is used as a key building block for the production of various organic compounds. Its reactivity and functional groups allow it to be incorporated into a wide range of molecules, making it a useful tool for chemists in designing and synthesizing new compounds.
Specific Application:
4-(HYDROXYMETHYL)BENZALDEHYDE DIMETHYL ACETAL was used in the synthesis of 5′-O-TBDPS-2′,3′-O-(4-hydroxymethyl-(1R)-benzyliden)-inosine, which is a complex organic molecule with potential applications in the pharmaceutical industry. The compound's unique structure and properties make it a valuable addition to the synthesis process, contributing to the development of new drugs and therapeutic agents.

InChI:InChI=1/C10H14O3/c1-12-10(13-2)9-5-3-8(7-11)4-6-9/h3-6,10-11H,7H2,1-2H3

Upstream product

• 42228-16-0 methyl 4-(dimethoxymethyl)benzoate 
• 187682-10-6 (+/-)-4-(3,4,5,6-tetrahydro-2H-pyran-2-yloxymethyl)benzaldehyde 
• 149-73-5 trimethyl orthoformate 
• 1571-08-0 methyl 4-formylbenzoate 
• 7732-18-5 water 
• 619-66-9 4-Carboxybenzaldehyde 
• 121-44-8 triethylamine 
• 77-76-9 2,2-dimethoxy-propane 

Downstream Products

• 73291-09-5 4-chloromethylbenzaldehyde 
• 183057-67-2 Benzoic acid 4-dimethoxymethyl-benzyl ester 
• 212780-31-9 (2S,3R)-3-[(3aR,4S,6R,7S,7aR)-7-Benzyloxy-2-(4-hydroxymethyl-phenyl)-4-methyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yloxy]-2-(9H-fluoren-9-ylmethoxycarbonylamino)-butyric acid allyl ester 
• 52010-97-6 4-(hydroxylmethyl)benzaldehyde 
• 907587-61-5 4-chloro-2-[(4-formylbenzyl)oxy]-N-phenylbenzenesulfonamide 
• 183058-00-6 (4R,5R)-2-[4-(bromomethyl)phenyl]-α,α,α',α'-tetraphenyl-1,3-dioxolane-4,5-dimethanol 
• 183184-06-7 (4S,5S)-2-(4-Benzoyloxymethyl-phenyl)-[1,3]dioxolane-4,5-dicarboxylic acid dimethyl ester 
• 183057-70-7 (4R,5R)-2-(4-Benzoyloxymethyl-phenyl)-[1,3]dioxolane-4,5-dicarboxylic acid dimethyl ester 
• 183057-89-8 [(4R,5R)-5-(Hydroxy-diphenyl-methyl)-2-(4-hydroxymethyl-phenyl)-[1,3]dioxolan-4-yl]-diphenyl-methanol 
• 1191248-89-1 2,6-Dichloro-4-(3-(4-(dimethoxymethyl)benzyloxy)-1,2,4-triazin-6-yl)phenol 
• 1221253-55-9 5'-O-TBDPS-2',3'-O-(4-hydroxymethylbenzylidene)inosine 

Relevant articles and documents

An efficient and versatile procedure for the synthesis of acetals from aldehydes and ketones catalyzed by lithium tetrafluoroborate

Acetals are obtained in good to excellent yields by treatment of aldehydes and ketones with trialkyl orthoformate and the corresponding alcohol in the presence of a catalytic amount of lithium tetrafluoroborate. Due to the mild reaction conditions, this method is compatible with acid-sensitive substrates.

Fuopeptide mimetics

Bioactive fucopeptides and libraries of fucopeptides having advanced activities against P-selectin as sialyl Lewis X mimetics with IC50 values in the low mM range are synthesized by solid phase synthesis using para-acyloxymethylenzlidene acetal (p-AMBA) a

146. Polymer- and dendrimer-bound Ti-TADDO lates in catalytic (and stoichiometric) enantioselective reactions: Are pentacoordinate cationic Ti complexes the catalytically active species?

α,α,α′,α′-Tetraaryl-1,3-dioxolane-4,5- dimethanols (TADDOLs), containing styryl groups either at C(2) of the heterocyclic ring or in the α-position, were prepared in the usual way (18-22, 24, 25). These compounds were copolymerized with styrene and divinylbenzene in a suspension, yielding polymers (33-40, Scheme 3) as beads with a rather uniform particle-size distribution (150-450 μm), swellable in common organic solvents, HOCH2- and BrCH2-substituted TADDOLs were also prepared and used for attachement to Merrifield resin or to dendritic molecules (23, 26-32). The TADDOL moieties in these materials are accessible to form Ti (and Al) complexes (Scheme 4) which can be used as polymer- or dendrimer-bound reagents (stoichiometric) or Lewis acids (catalytic). The reactions studied with these new chiral auxiliaries are: enantioselective nucleophilic additions to aldehydes (of R2Zn and RTi(OCHMe2)3; Schemes, Table 1) and to ketones (of LiAlH4, Table 2); enantioselective ring opening of meso-anhydrides (Scheme 6); [4+2] and [3+2] cycloadditions of 3-crotonyl-1,3-oxazolidin-2-one to cyclopentadiene and to (Z)-N-benzylidenephenylamine N-oxide (→ 48, 9, Scheme 7, Tables 3, , and Fig. ). The enantioselectivities reached with most of the polymer-bound or dendritic TADDOL ligands were comparable or identical to those observed with the soluble analogs. The activity of the polymer-bound Lewis acids was only slightly reduced as compared with that encountered under homogeneous conditions. Multiple use of the beads (up to 10 times), without decreased performance, has been demonstrated (Figs. 3 and 4). The poorer selectivity in the Diets-Alder reaction (Scheme 7a), induced by the polymer-bound Cl2Ti-TADDOLate as compared to the soluble one, is taken as an opportunity to discuss the mechanism of this Lewis-acid catalysis, and to propose a cationic, trigonal-bi-pyramidal complex as the catalytically active species (Fig. 6) It is suggested that similar cations may be involved in other Ti-TADDOLate-mediated reactions as well.