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56977-08-3

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56977-08-3 Usage

Description

1,5-Dibenzyl Glutarate, with the CAS number 56977-08-3, is a colorless oil compound that is primarily utilized in the field of organic synthesis. It is a versatile chemical intermediate that can be employed in the creation of various complex organic molecules.

Uses

Used in Organic Synthesis:
1,5-Dibenzyl Glutarate is used as a chemical intermediate for the synthesis of a wide range of organic compounds. Its unique structure and properties make it a valuable building block in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
1,5-Dibenzyl Glutarate is used as a key component in the development of new drugs and therapeutic agents. Its versatility in organic synthesis allows for the creation of novel molecular structures with potential applications in treating various diseases and medical conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 1,5-Dibenzyl Glutarate is used as a starting material for the synthesis of various pesticides, herbicides, and other crop protection agents. Its chemical properties make it suitable for the development of effective and environmentally friendly solutions for agricultural challenges.
Used in Specialty Chemicals:
1,5-Dibenzyl Glutarate is also used in the production of specialty chemicals, such as additives, coatings, and polymers. Its unique properties contribute to the development of innovative materials with specific applications in various industries, including automotive, electronics, and construction.

Check Digit Verification of cas no

The CAS Registry Mumber 56977-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,7 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56977-08:
(7*5)+(6*6)+(5*9)+(4*7)+(3*7)+(2*0)+(1*8)=173
173 % 10 = 3
So 56977-08-3 is a valid CAS Registry Number.

56977-08-3SDS

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 dibenzyl pentanedioate

1.2 Other means of identification

Product number -
Other names 1,5-DIBENZYL GLUTARATE

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:56977-08-3 SDS

56977-08-3Relevant articles and documents

ZWITTERIONIC CATALYSTS FOR (TRANS)ESTERIFICATION: APPLICATION IN FLUOROINDOLE-DERIVATIVES AND BIODIESEL SYNTHESIS

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Paragraph 0018; 0030, (2021/01/29)

An amide/iminium zwitterion catalyst has a catalyst pocket size that promotes transesterification and dehydrative esterification. The amide/iminium zwitterions are easily prepared by reacting aziridines with aminopyridines. The reaction can be applied a wide variety of esterification processes including the large-scale synthesis of biodiesel. The amide/iminium zwitterions allow the avoidance of strongly basic or acidic condition and avoidance of metal contamination in the products. Reactions are carried out at ambient or only modestly elevated temperatures. The amide/iminium zwitterion catalyst is easily recycled and reactions proceed in high to quantitative yields.

PROCESS FOR DOUBLE CARBONYLATION OF ALLYL ALCOHOLS TO CORRESPONDING DIESTERS

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Paragraph 0064; 0073; 0074, (2017/07/14)

The invention relates to a process for doubly carbonylating allyl alcohols to the corresponding diesters, wherein a linear or branched allyl alcohol is reacted with a linear or branched alkanol (alcohol) with supply of CO and in the presence of a catalytic system composed of a palladium complex and at least one organic phosphorus ligand and in the presence of a hydrogen halide selected from HCl, HBr and HI.

Esterification of dicarboxylic acids with benzyl alcohol under the action of the microwave radiation

Aver'yanov,Batrakova,Samuilov,Spiridonova,Kochnev,Galibeev,Gnezdilov

experimental part, p. 1920 - 1923 (2009/02/08)

Reaction of dicarboxylic acid with benzyl alcohol under the microwave irradiation proceeds faster as compared to the thermal conditions. The main reaction products are alkyl dicarboxylates, and the monoester and dibenzyl ether are formed as the side products. A proposal about the nature of the nonthermal effect in the reactions stimulated by the microwave irradiation is considered.

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