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Sebacic acid, diphenyl ester, also known as diphenyl sebacate, is an organic compound with the chemical formula C22H22O4. It is a colorless, crystalline solid that is derived from the esterification of sebacic acid and phenol. SEBACICACID,DIPHENYLESTER is widely used in the production of various plasticizers, particularly for cellulose derivatives such as cellulose acetate and cellulose nitrate. Diphenyl sebacate is valued for its low volatility, high boiling point, and excellent electrical properties, making it suitable for applications in the plastics, coatings, and adhesives industries. It also serves as a solvent and a component in the formulation of some types of lubricants and personal care products.

2918-18-5

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2918-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2918-18-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2918-18:
(6*2)+(5*9)+(4*1)+(3*8)+(2*1)+(1*8)=95
95 % 10 = 5
So 2918-18-5 is a valid CAS Registry Number.

2918-18-5SDS

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 diphenyl sebacate

1.2 Other means of identification

Product number -
Other names Sebacinsaeure-diphenylester

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:2918-18-5 SDS

2918-18-5Relevant academic research and scientific papers

Photo-on-Demand Synthesis of Vilsmeier Reagents with Chloroform and Their Applications to One-Pot Organic Syntheses

Liang, Fengying,Eda, Kazuo,Okazoe, Takashi,Wada, Akihiro,Mori, Nobuaki,Konishi, Katsuhiko,Tsuda, Akihiko

, p. 6504 - 6517 (2021/05/06)

The Vilsmeier reagent (VR), first reported a century ago, is a versatile reagent in a variety of organic reactions. It is used extensively in formylation reactions. However, the synthesis of VR generally requires highly toxic and corrosive reagents such as POCl3, SOCl2, or COCl2. In this study, we found that VR is readily obtained from a CHCl3 solution containing N,N-dimethylformamide or N,N-dimethylacetamide upon photo-irradiation under O2 bubbling. The corresponding Vilsmeier reagents were obtained in high yields with the generation of gaseous HCl and CO2 as byproducts to allow their isolations as crystalline solid products amenable to analysis by X-ray crystallography. With the advantage of using CHCl3, which bifunctionally serves as a reactant and a solvent, this photo-on-demand VR synthesis is available for one-pot syntheses of aldehydes, acid chlorides, formates, ketones, esters, and amides.

Doubly Strapped Redox-Switchable 5,10,15,20-Tetraaryl-5,15-diazaporphyrinoids: Promising Platforms for the Evaluation of Paratropic and Diatropic Ring-Current Effects

Ochiai, Hikari,Furukawa, Ko,Nakano, Haruyuki,Matano, Yoshihiro

, p. 2283 - 2296 (2021/02/05)

This paper presents a novel series of chemically stable and redox-switchable 20π, 19π, and 18π5,10,15,20-tetraaryl-5,15-diazaporphyrinoids (TADAPs) that have two alkyl-chain straps above and below the diazaporphyrin ring. Three types of doubly strapped TA

Base catalyzed sustainable synthesis of phenyl esters from carboxylic acids using diphenyl carbonate

Kreye, Oliver,Meier, Michael A. R.

, p. 53155 - 53160 (2015/06/25)

Phenyl esters were obtained in moderate to high yields by reaction of aliphatic and aromatic carboxylic acids with one equivalent of diphenyl carbonate in the presence of catalytic amounts of tertiary amine bases, such as DBU, TBD and DMAP under neat conditions at elevated temperatures (>100°C).

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