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Benzene, 1-(diethoxymethyl)-2-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88356-11-0

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88356-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88356-11-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,5 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88356-11:
(7*8)+(6*8)+(5*3)+(4*5)+(3*6)+(2*1)+(1*1)=160
160 % 10 = 0
So 88356-11-0 is a valid CAS Registry Number.

88356-11-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(diethoxymethyl)-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names 2-nitro-benzaldehyde 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:88356-11-0 SDS

88356-11-0Relevant academic research and scientific papers

Practical acetalization and transacetalization of carbonyl compounds catalyzed by recyclable PVP-I

Cao, Fu-Rong,Lu, Guangying,Ren, Jiangmeng,Wang, Di,Zeng, Bu-Bing

, (2021/06/21)

A novel PVP-I catalyzed acetalizations/transacetalizations of carbonyl compounds has been developed processing with a mild and easy handling fashion. Different types of Acyclic and cyclic acetals were prepared from carbonyl compounds or their acetals successfully. Further applications of newly developed catalytic combination were testified. This protocol featured with simplicity of operation, mild reaction condition, short reaction time, recyclable of catalyst and broad substrates scope with excellent yields.

Tropylium salts as efficient organic Lewis acid catalysts for acetalization and transacetalization reactions in batch and flow

Lyons,Crocker,Enders,Nguyen

supporting information, p. 3993 - 3996 (2017/09/08)

Acetalization reactions play significant roles in the synthetically important masking chemistry of carbonyl compounds. Herein we demonstrate for the first time that tropylium salts can act as organic Lewis acid catalysts to facilitate acetalization and transacetalization reactions of a wide range of aldehyde substrates. This metal-free method works efficiently in both batch and flow conditions, prompting further future applications of tropylium organocatalysts in green synthesis.

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.

Gallium triiodide as a highly efficient and mild catalyst for the diethyl acetalization of carbonyl compounds

Ding, Jin-Chang,Xu, Rong,Liu, Miao-Chang,Chen, Xi-An,Wu, Hua-Yue

experimental part, p. 566 - 568 (2009/07/18)

Diethyl acetals were obtained from carbonyl compounds in good to excellent yields under mild reaction conditions in the presence of triethyl orthoformate and a catalytic amount of gallium triiodide in anhydrous ethanol.

Cobalt(II)-catalyzed chemoselective synthesis of acetals from aldehydes

Velusamy, Subbarayan,Punniyamurthy

, p. 4917 - 4920 (2007/10/03)

The acetalization of aldehydes has been studied with methanol, ethanol, and 2-propanol using CoCl2 in high yields under reflux conditions. The reaction is simple, efficient, chemoselective and does not involve any other additive.

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.

A new molecular iodine-catalyzed acetalization of carbonyl compounds

Basu, Manas K.,Samajdar, Susanta,Becker, Frederick F.,Banik, Bimal K.

, p. 319 - 321 (2007/10/03)

A new and facile molecular iodine-catalyzed acetalization of carbonyl compounds has been developed. Useful selectivity has also been demonstrated.

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