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4-(diethoxymethyl)phenol, with the molecular formula C11H16O3, is an aromatic phenol derivative characterized by its colorless to pale yellow liquid appearance and a pleasant odor. It is soluble in organic solvents such as ethanol and ether, and is recognized for its adhesive and bonding properties, making it a versatile intermediate in the production of pharmaceuticals and other organic compounds.

7465-16-9

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7465-16-9 Usage

Uses

Used in Pharmaceutical Industry:
4-(diethoxymethyl)phenol is used as an intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicinal compounds.
Used in Adhesive and Coating Formulation:
4-(diethoxymethyl)phenol is used as a crosslinking agent in the formulation of adhesives, coatings, and sealants, enhancing their adhesive and bonding properties.
Used in Polymer and Resin Synthesis:
Due to its reactivity and versatility, 4-(diethoxymethyl)phenol is utilized in the synthesis of various polymers and resins, playing a crucial role in the development of a wide range of industrial and commercial products.

Check Digit Verification of cas no

The CAS Registry Mumber 7465-16-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7465-16:
(6*7)+(5*4)+(4*6)+(3*5)+(2*1)+(1*6)=109
109 % 10 = 9
So 7465-16-9 is a valid CAS Registry Number.

7465-16-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(diethoxymethyl)phenol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7465-16-9 SDS

7465-16-9Downstream Products

7465-16-9Relevant academic research and scientific papers

Preparation method of 3-bromo-4-hydroxybenzaldehyde

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Paragraph 0036-0038, (2020/02/19)

The invention discloses a preparation method of 3-bromo-4-hydroxybenzaldehyde. The preparation method comprises the following steps: (1) carrying out a bromination reaction on p-hydroxybenzene methylal and bromine to obtain 3-bromo-4-hydroxybenzene methylal; and (2) carrying out a hydrolysis reaction on the 3-bromo-4-hydroxybenzene methylal obtained in the step (1), and carrying out post-treatmentafter the reaction is finished to obtain the 3-bromo-4-hydroxybenzaldehyde. According to the preparation method, aldehyde is replaced with acetal for the bromination reaction, so that generation of adibromo product is effectively avoided, the yield and purity of a monobromo product are improved, and industrialization is facilitated.

A facile and efficient protocol for esterification and acetalization in a PEG1000-D(A)IL/toluene thermoregulated catalyst-media combined systems

Wang, Yinglei,Zhi, Huizhen,Luo, Jun

, p. 46 - 52 (2013/09/23)

A novel efficient and recyclable temperature-dependent biphasic catalyst and reaction media combined system comprised of PEG-1000 linked dicationic acidic ionic liquid and toluene was developed and applied in esterification of aromatic acids and acetalization of aromatic aldehydes with good to excellent yields. This system is characteristic of temperature-dependent reversible biphasic property, simple and facile recyclability, high catalytic activity and extensive substrate and reaction adaptability.

Bronsted acidic ionic liquids as efficient and recyclable catalysts for protection of carbonyls to acetals and ketals under mild conditions

Du, Yuying,Tian, Fuli

, p. 2703 - 2708 (2007/10/03)

A series of acidic ionic liquids have been used as efficient catalysts for the protection of various carbonyl compounds at room temperature. The features of mild conditions, satisfactory isolated yield, simple workup, and the recyclability of the catalyst were present in this process. Copyright Taylor & Francis, Inc.

Sulfamic acid as a cost-effective and recyclable catalyst for protection of carbonyls to acetals and ketals under mild conditions

Gong, Weizhong,Wang, Bo,Gu, Yanglong,Yan, Liang,Yang, Liming,Suo, Jishuan

, p. 4243 - 4247 (2007/10/03)

An efficient H2NSO3H-catalyzed protection of various carbonyl compounds at room temperature was investigated. The features of mild conditions, cost-efficient catalyst, simple workup, and the recyclability of the catalyst were represented in this process.

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

Hamada, Nao,Kazahaya, Kiyoshi,Shimizu, Hisashi,Sato, Tsuneo

, p. 1074 - 1076 (2015/10/07)

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.

Tetrabutylammonium tribromide (TBATB) as an efficient generator of HBr for an efficient chemoselective reagent for acetalization of carbonyl compounds

Gopinath, Rangam,Haque, Sk. Jiaul,Patel, Bhisma K.

, p. 5842 - 5845 (2007/10/03)

Acyclic and cyclic acetals of various carbonyl compounds were obtained in excellent yields under a mild reaction condition in the presence of trialkyl orthoformate and a catalytic amount of tetrabutylammonium tribromide (TBATB) in absolute alcohol. Chemoselective acetalization of an aldehyde in the presence of ketone, unsymmetrical acetal formation, shorter reaction times, mild reaction conditions, the stability of acid-sensitive protecting groups, high efficiencies, facile isolation of the desired products, and the catalytic nature of the reagent make the present methodology a practical alternative.

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