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Benzoic acid, 4-chloro-, methylene ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56741-11-8

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56741-11-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56741-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,7,4 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56741-11:
(7*5)+(6*6)+(5*7)+(4*4)+(3*1)+(2*1)+(1*1)=128
128 % 10 = 8
So 56741-11-8 is a valid CAS Registry Number.

56741-11-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methylidene di(4-chlorobenzoate)

1.2 Other means of identification

Product number -
Other names bis(4-chlorobenzoyloxy)methane

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:56741-11-8 SDS

56741-11-8Relevant academic research and scientific papers

Dichloromethane as a methylene synthon for regioselective linkage of diverse carboxylic acids: Direct access to methylene diesters under metal-free conditions

Wang, Shuiliang,Fu, Zhengjiang,Huang, Zhicong,Jiang, Yongqing,Guo, Shengmei,Cai, Hu

supporting information, p. 1173 - 1177 (2019/05/07)

A metal-free cross coupling between common CH2Cl2 and carboxylic acids has been achieved with K2CO3 as the sole additive. This simple protocol is a convenient and cost-effective route to synthesize methylene die

Synthesis of esters from aldehydes or carboxylic acids with dichloromethane, dichloroethane or dichloropropane under mild conditions

Lin, Feng,Feng, Qiang,Cui, Xiuling,Song, Qiuling

, p. 20246 - 20253 (2013/11/06)

Dichloromethane (DCM) as a C1 source has been discovered: methylene diesters from DCM and carboxylic acids or aldehydes with TBHP in water were efficiently synthesized. The reactions proceed under mild conditions and afford both aliphatic and aromatic met

The chemistry of acylals. Part I. The reactivity of acylals towards Grignard and organolithium reagents

Sydnes, Leiv K.,Sandberg, Marcel

, p. 12679 - 12690 (2007/10/03)

Aldehyde acylals have been prepared and reacted with Grignard and alkyllithium reagents. Acylals from formaldehyde furnished complex reaction mixtures when reacted with both reagents. Acylals of other aldehydes gave reaction mixtures that consisted mainly of an ester, generated by replacing one of the carboxy groups with the organic part of the organometallic reagent, and regenerated aldehyde. The esters were formed in the highest yields. Yields above 90% were experienced when the acylals were reacted with Grignard reagents under Barbier conditions.

Efficient method for synthesis of methylene diesters using polyethylene glycol as a phase transfer catalyst

Kavitake, Bhanudas P.,Salunkhe, Manikrao M.,Wadgaonkar, Prakash P.

, p. 1703 - 1710 (2007/10/03)

Methylene diesters were synthesized in high yields at room temperature by reacting the potassium salt of a carboxylic acid with dibromo methane under the conditions of solid-liquid phase transfer catalysis using poly (ethylene glycol)-600 (PEG-600) as the

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