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3-OXO-3-(3,4,5-TRIMETHOXYPHENYL)PROPIONIC ACID METHYL ESTER is a chemical compound with the molecular formula C13H18O6. It is an ester derivative of 3-oxo-3-(3,4,5-trimethoxyphenyl)propionic acid, known for its structural properties and reactivity.
Used in Pharmaceutical Industry:
3-OXO-3-(3,4,5-TRIMETHOXYPHENYL)PROPIONIC ACID METHYL ESTER is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs and therapies.
Used in Organic Chemistry Research:
3-OXO-3-(3,4,5-TRIMETHOXYPHENYL)PROPIONIC ACID METHYL ESTER is used as a reagent in organic chemistry research to explore its potential applications and reactions in the creation of various organic compounds.
Used in Drug Development:
3-OXO-3-(3,4,5-TRIMETHOXYPHENYL)PROPIONIC ACID METHYL ESTER is used as a component in drug development, leveraging its structural properties to enhance the discovery and design of novel therapeutic agents.
Used in Biotechnology Industry:
3-OXO-3-(3,4,5-TRIMETHOXYPHENYL)PROPIONIC ACID METHYL ESTER may have applications in the biotechnology industry, where it could be utilized in the research and development of innovative biotechnological solutions and products.

139148-39-3

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139148-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139148-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,1,4 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 139148-39:
(8*1)+(7*3)+(6*9)+(5*1)+(4*4)+(3*8)+(2*3)+(1*9)=143
143 % 10 = 3
So 139148-39-3 is a valid CAS Registry Number.

139148-39-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-OXO-3-(3,4,5-TRIMETHOXYPHENYL)PROPIONIC ACID METHYL ESTER

1.2 Other means of identification

Product number -
Other names Methyl 3-(3,4,5-trimethoxyphenyl)-3-oxopropionate

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:139148-39-3 SDS

139148-39-3Relevant academic research and scientific papers

Expedient synthesis of 3-hydroxyisoquinolines and 2-hydroxy-1,4- naphthoquinones via one-pot aryne acyl-alkylation/condensation

Allan, Kevin M.,Hong, Boram D.,Stoltz, Brian M.

supporting information; experimental part, p. 4960 - 4964 (2010/02/15)

A convenient method is disclosed for the synthesis of both 3-hydroxyisoquinolines and 2-hydroxy-1,4-naphthoquinones from β-ketoesters using a one-pot aryne acyl-alkylation/condensation procedure. When performed in conjunction with a one-step method for the synthesis of the β-ketoester substrates, this method provides a new route to these polyaromatic structures in only two steps from commercially available carboxylic acid starting materials. The utility of this approach is demonstrated in the synthesis of the atropisomeric P,N-ligand, QUINAP. The Royal Society of Chemistry 2009.

Discovery and structure-activity relationships of trisubstituted pyrimidines/pyridines as novel calcium-sensing receptor antagonists

Yang, Wu,Ruan, Zheming,Wang, Yufeng,Van Kirk, Katy,Zhengping, Ma.,Arey, Brian J.,Cooper, Christopher B.,Seethala, Ramakrishna,Feyen, Jean H. M.,Dickson Jr., John K.

supporting information; experimental part, p. 1204 - 1208 (2009/12/25)

The trisubstituted pyrimidine 1 was identified through high-throughput screening as a novel calcium-sensing receptor (CaSR) antagonist. Small molecule CaSR antagonists and/or negative allosteric modulators have the potential to act as an anabolic agent for the treatment of osteoporosis. The investigation of structure-activity relationships around 1 resulted in the identification of 18c and 18d, which showed efficacy at promoting PTH release in vivo and exhibited improved potency and solubility over the original lead 1.

TRISUBSTITUTED HETEROAROMATIC COMPOUNDS AS CALCIUM SENSING RECEPTOR MODULATORS

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Page 38, (2010/02/09)

Trisubstituted heteroaromatic compounds having the structure Formula (I) are provided, wherein X is C or N; A and B are each independently CH or N, with the proviso that A and B cannot both be CH; R is Ar-L-; R is hydrogen or alkyl; or R and R can be joined together to form a 4- to 7-membered cycloheteroalkyl ring; R to R, Ar and L are as defined herein. A method for using these compounds to treat diseases associated with abnormal bone or mineral homeostasis is also provided.

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