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Pentanedioic acid, 2-phenyl-, 1-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

121925-63-1

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121925-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121925-63-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,9,2 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 121925-63:
(8*1)+(7*2)+(6*1)+(5*9)+(4*2)+(3*5)+(2*6)+(1*3)=111
111 % 10 = 1
So 121925-63-1 is a valid CAS Registry Number.

121925-63-1SDS

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 5-ethoxy-5-oxo-4-phenylpentanoate

1.2 Other means of identification

Product number -
Other names Pentanedioic acid,2-phenyl-,1-ethyl ester

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:121925-63-1 SDS

121925-63-1Downstream Products

121925-63-1Relevant academic research and scientific papers

Synthesis of α-substituted cyclobutane β-keto esters

Kortmann,Westermann

, p. 931 - 933 (2007/10/02)

The title compounds, α-substituted-β-keto esters 4, were prepared from suitably substituted cyclopropylideneacetates 2 by epoxidation and Wagner-Meerwein rearrangement. The highly strained oxaspiro[2.2]pentane intermediate 3 was isolated.

HIGHLY REGIOSELECTIVE RING-OPENING OF α-SUBSTITUTED CYCLIC ACID ANHYDRIDES CATALYZED BY LIPASE

Hiratake, Jun,Yamamoto, Kazuyoshi,Yamamoto, Yukio,Oda, Jun'ichi

, p. 1555 - 1556 (2007/10/02)

Lipase Amano P irreversibly catalyzed a ring-opening of α-substituted cyclic acid anhydrides 1 preferentially at the less hindered carbonyl group to give monoesters with high regioselectivity.

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