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1270914-58-3

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1270914-58-3 Usage

Description

Methyl 3-((2-aminophenyl)amino)propanoate is a chemical compound with the molecular formula C11H15NO2. It is a white crystalline powder that is a derivative of propanoic acid with a methyl ester group and an amino group attached to the phenyl ring. methyl 3-((2-aminophenyl)amino)propanoate is used in the pharmaceutical industry as a precursor in the synthesis of various drugs and pharmaceuticals. Its presence as a potential substrate for enzymatic reactions and its possible biological activity in certain contexts make it a valuable compound in organic synthesis and as a chemical intermediate in the production of other compounds.

Uses

Used in Pharmaceutical Industry:
Methyl 3-((2-aminophenyl)amino)propanoate is used as a precursor in the synthesis of various drugs and pharmaceuticals for its ability to be a building block in creating complex molecular structures.
Used in Organic Synthesis:
Methyl 3-((2-aminophenyl)amino)propanoate is used as a reagent in organic synthesis, facilitating the creation of a wide range of chemical compounds due to its versatile molecular structure.
Used as a Chemical Intermediate:
In the production of other compounds, methyl 3-((2-aminophenyl)amino)propanoate serves as a chemical intermediate, playing a crucial role in the synthesis of various end products.
Used in Enzymatic Reactions:
The presence of the amino group in methyl 3-((2-aminophenyl)amino)propanoate makes it a potential substrate for enzymatic reactions, which can be harnessed for specific biological or chemical processes.
Used for Biological Activity:
Methyl 3-((2-aminophenyl)amino)propanoate may exhibit biological activity in certain contexts, making it a candidate for further research and development in the field of biochemistry and pharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 1270914-58-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,0,9,1 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1270914-58:
(9*1)+(8*2)+(7*7)+(6*0)+(5*9)+(4*1)+(3*4)+(2*5)+(1*8)=153
153 % 10 = 3
So 1270914-58-3 is a valid CAS Registry Number.

1270914-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-((2-aminophenyl)amino)propanoate

1.2 Other means of identification

Product number -
Other names -

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:1270914-58-3 SDS

1270914-58-3Relevant articles and documents

Discovery of Benzotriazolo[4,3-d][1,4]diazepines as Orally Active Inhibitors of BET Bromodomains

Taylor, Alexander M.,Vaswani, Rishi G.,Gehling, Victor S.,Hewitt, Michael C.,Leblanc, Yves,Audia, James E.,Bellon, Steve,Cummings, Richard T.,Co?té, Alexandre,Harmange, Jean-Christophe,Jayaram, Hari,Joshi, Shivangi,Lora, Jose M.,Mertz, Jennifer A.,Neiss, Adrianne,Pardo, Eneida,Nasveschuk, Christopher G.,Poy, Florence,Sandy, Peter,Setser, Jeremy W.,Sims, Robert J.,Tang, Yong,Albrecht, Brian K.

supporting information, p. 145 - 150 (2016/03/01)

Inhibition of the bromodomains of the BET family, of which BRD4 is a member, has been shown to decrease myc and interleukin (IL) 6 in vivo, markers that are of therapeutic relevance to cancer and inflammatory disease, respectively. Herein we report substituted benzo[b]isoxazolo[4,5-d]azepines and benzotriazolo[4,3-d][1,4]diazepines as fragment-derived novel inhibitors of the bromodomain of BRD4. Compounds from these series were potent and selective in cells, and subsequent optimization of microsomal stability yielded representatives that demonstrated dose- and time-dependent reduction of plasma IL-6 in mice.

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