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Benzenepropanoic acid, a-[(3-methoxyphenyl)methyl]-b-oxo-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

867214-92-4

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867214-92-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 867214-92-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,7,2,1 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 867214-92:
(8*8)+(7*6)+(6*7)+(5*2)+(4*1)+(3*4)+(2*9)+(1*2)=194
194 % 10 = 4
So 867214-92-4 is a valid CAS Registry Number.

867214-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methoxybenzyl)-3-oxo-3-phenylpropionic acid ethyl ester

1.2 Other means of identification

Product number -
Other names ethyl 2-(3-methoxybenzyl)-3-oxo-3-phenylpropanoate

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:867214-92-4 SDS

867214-92-4Relevant academic research and scientific papers

Heck reaction of Baylis-Hillman adducts with iodobenzenes using a catalytic amount of Pd/C under solvent-free conditions

Kim, Hyun-Soo,Lee, Sang-Jin,Choi, Boram,Yoon, Cheol Min

, p. 3161 - 3164 (2012/11/13)

The reaction of Baylis-Hillman adducts with iodobenzenes using commercially available palladium-on-carbon as a catalyst under solvent-free conditions afforded the corresponding coupling products, α-benzyl-β-keto esters, in high to excellent yields. The reactions are very efficient.

Indenone derivatives: A novel template for peroxisome proliferator- activated receptor γ (PPARγ) agonists

Ahn, Jin Hee,Shin, Mi Sik,Jung, Sun Ho,Kang, Seung Kyu,Kim, Kwang Rok,Rhee, Sang Dal,Jung, Won Hoon,Yang, Sung Don,Kim, Seung Jun,Woo, Joo Rang,Lee, Jeong Hyung,Cheon, Hyae Gyeong,Kim, Sung Soo

, p. 4781 - 4784 (2007/10/03)

Agonists of peroxisome proliferator-activated receptor γ(PPAR γ) are of interest as a treatment for diabetes, which prompted the identification of a new class of non-TZD PPAR γ agonist. Moreover, compound 14c has displayed the most active agonistic activi

INDENE DERIVATIVES AND PROCESS FOR THE PREPARATION THEREOF

-

Page/Page column 21, (2008/06/13)

The inventive indene derivatives of formula (I) are capable of selectively modulating the activities of peroxisome proliferator activated receptors (PPARs), causing no adverse side effects, and thus, they are useful for the treatment and prevention of dis

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