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Phenol, 2-(diethoxymethyl)-, also known as 2-(Diethoxymethyl)phenol or Phenol, 2-(2-methoxyethoxy)-, is an organic compound with the chemical formula C11H16O3. It is a colorless to pale yellow liquid with a molecular weight of 192.24 g/mol. Phenol, 2-(diethoxymethyl)- is characterized by a phenol group (C6H5OH) with a diethoxymethyl group (CH3CH2OCH2CH2O-) attached to the 2-position of the phenol ring. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and potential applications, Phenol, 2-(diethoxymethyl)- is an important chemical in the field of organic synthesis.

6842-31-5

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6842-31-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6842-31-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,4 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6842-31:
(6*6)+(5*8)+(4*4)+(3*2)+(2*3)+(1*1)=105
105 % 10 = 5
So 6842-31-5 is a valid CAS Registry Number.

6842-31-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(diethoxymethyl)phenol

1.2 Other means of identification

Product number -
Other names Salicylaldehyd-diethylacetal

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:6842-31-5 SDS

6842-31-5Relevant academic research and scientific papers

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.

BETA-BLOCKING SUBSTITUTED IMIDAZOLES

-

, (2008/06/13)

Novel substituted imidazoles and methods for their preparation are disclosed. These imidazoles, and their salts, exhibit pharmacological activity which includes antihypertensive activity and β-adrenergic blocking activity.

BETA-ADRENERGIC BLOCKING IMIDAZOLYLPHENOXY PROPANOLAMINES

-

, (2008/06/13)

Substituted imidazoles and methods for their preparation are disclosed. These imidazoles, and their salts, exhibit pharmacological activity which includes antihypertensive activity and β-adrenergic blocking activity. STR1

Acetal Formation Facilitated in 2-Hydroxyaryl Aldehydes by Intramoleculedar Acyl Group Transfer

Liepa, Andris J.,Morton, Trevor C.

, p. 1747 - 1757 (2007/10/02)

Convenient preparations of synthetically useful acetals, a dithioacetal and an oxathiolan from the 2-acyl derivatives of 2-hydroxyaryl aldehydes under basic conditions are described.The mildness of the reaction conditions is illustrated by the formation of an ethoxycarbonyl-substituted dioxolan.The reaction is dependent upon an intramolecular acetyl group transfer and the mechanism of the reaction is discussed.Some broader implications of this type of acyl transfer are discussed.

3-AMINO-2-HYDROXYPROPOXYARYL IMIDAZOLE DERIVATIVES

-

, (2008/06/13)

Novel substituted imidazoles of the formula STR1 and methods for their preparation are disclosed. These imidazoles, and their salts, exhibit pharmacological activity which includes antihypertensive activity and β-adrenergic blocking activity.

3-AMINO-2-OR-PROPOXYARYL SUBSTITUTED IMIDAZOLES

-

, (2008/06/13)

Novel 3-amino-2-OR-propoxyaryl substituted imidazoles and methods for their preparation are disclosed. These imidazoles, and their salts, exhibit pharmacological activity which includes antihypertensive activity and β-adrenergic blocking activity.

Phenyl carbamates

-

, (2008/06/13)

O-Phenylcarbamates, e.g. those of the formula EQU1 are biocides, e.g. insecticides.

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