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diphenyl pentanedioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 47172-89-4 Structure
  • Basic information

    1. Product Name: diphenyl pentanedioate
    2. Synonyms:
    3. CAS NO:47172-89-4
    4. Molecular Formula: C17H16O4
    5. Molecular Weight: 284.3065
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 47172-89-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 432.6°C at 760 mmHg
    3. Flash Point: 218.2°C
    4. Appearance: N/A
    5. Density: 1.174g/cm3
    6. Vapor Pressure: 1.09E-07mmHg at 25°C
    7. Refractive Index: 1.555
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: diphenyl pentanedioate(CAS DataBase Reference)
    11. NIST Chemistry Reference: diphenyl pentanedioate(47172-89-4)
    12. EPA Substance Registry System: diphenyl pentanedioate(47172-89-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 47172-89-4(Hazardous Substances Data)

47172-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 47172-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,1,7 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 47172-89:
(7*4)+(6*7)+(5*1)+(4*7)+(3*2)+(2*8)+(1*9)=134
134 % 10 = 4
So 47172-89-4 is a valid CAS Registry Number.

47172-89-4SDS

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 pentanedioate

1.2 Other means of identification

Product number -
Other names Diphenyl-glutarat

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:47172-89-4 SDS

47172-89-4Relevant articles and documents

Direct esterification of succinic acid with phenol using zeolite beta catalyst

Le, Son Dinh,Nishimura, Shun,Ebitani, Kohki

, p. 20 - 23 (2019/01/16)

Direct esterification of succinic acid with phenol in the presence of zeolite catalysts was explored. H+-zeolite β (SiO2/Al2O3 = 150) has emerged as the most effective solid acid catalyst, affording 96% yield of

A Two-Directional Synthesis of (+)-β-Isosparteine

Al-Saffar, Firas M.,Brown, Richard C. D.

, p. 3502 - 3504 (2017/07/15)

A two-directional synthesis of (+)-β-isosparteine is described in five steps from glutaric acid, where the entire carbon and nitrogen backbone of the alkaloid, possessing the requisite relative and absolute stereochemistry at its four stereogenic centers, is assembled using a double imino-aldol reaction.

O-acylation of substituted phenols with various alkanoyl chlorides under phase-transfer catalyst conditions

Simion, Alina Marieta,Hashimoto, Iwao,Mitoma, Yoshiharu,Egashira, Naoyoshi,Simion, Cristian

experimental part, p. 921 - 931 (2012/02/01)

Esterification of several types of mono-and disubstituted phenols with various mono-and dialkanoyl chlorides was performed in phase-transfer catalysis conditions, using tetrabutylammonium chloride in a mixture of aqueous NaOH and dichloromethane. The process is particularly efficient (almost quantitative yields) as well as rapid (only 5 min reaction time, at a temperature of0°C). Taylor & Francis Group, LLC.

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