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Butanedioic acid, (1-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 19263-14-0 Structure
  • Basic information

    1. Product Name: Butanedioic acid, (1-phenylethyl)-
    2. Synonyms:
    3. CAS NO:19263-14-0
    4. Molecular Formula: C12H14O4
    5. Molecular Weight: 222.241
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 19263-14-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Butanedioic acid, (1-phenylethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Butanedioic acid, (1-phenylethyl)-(19263-14-0)
    11. EPA Substance Registry System: Butanedioic acid, (1-phenylethyl)-(19263-14-0)
  • 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: 19263-14-0(Hazardous Substances Data)

19263-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19263-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,6 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19263-14:
(7*1)+(6*9)+(5*2)+(4*6)+(3*3)+(2*1)+(1*4)=110
110 % 10 = 0
So 19263-14-0 is a valid CAS Registry Number.

19263-14-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-phenylethyl)butanedioic acid

1.2 Other means of identification

Product number -
Other names 2-(1-phenylethyl)succinic acid

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:19263-14-0 SDS

19263-14-0Downstream Products

19263-14-0Relevant articles and documents

Decatungstate as photoredox catalyst: Benzylation of electron-poor olefins

Montanaro, Sara,Ravelli, Davide,Merli, Daniele,Fagnoni, Maurizio,Albini, Angelo

supporting information; experimental part, p. 4218 - 4221 (2012/09/22)

Excited tetrabutylammonium decatungstate (TBADT), known to activate a variety of compounds via hydrogen atom transfer (HAT), has now been applied as a photoredox catalyst for the effective oxidative cleavage of benzyl silanes and radical benzylation of reducible olefins occurring in isolated yields from poor to excellent.

"ONE-POT" SYNTHESIS OF DISYMMETRICALLY α,α'-DISUBSTITUTED SUCCINIC ANHYDRIDES PRECURSORS

Dana, A.,Campagnole, M.,Bourgeois, M.J.,Montaudon, E.

, p. 2981 - 2988 (2007/10/03)

A "one-pot" synthesis for disymmetrically α,α'-disubstituted succinic anhydrides precursors isreported in the present paper.Substituents are aryl, primary or secondary alkyl groups.This reaction represents a simple and quick method with fair yields.

Samarium(II) iodide - HMPA: A very efficient system for the selective reduction of α,β,-unsaturated carbonyl compounds

Cabrera,Alper

, p. 5007 - 5008 (2007/10/02)

α,β,-unsaturated esters, acids, and an anhydride undergo efficient double bond reduction by SmI2/HMPA in tetrahydrofuran.

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