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117011-70-8

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117011-70-8 Usage

General Description

The chemical 2-(4-Aminophenoxy)-2-methylpropionic acid is a compound with the molecular formula C11H15NO3. It is a derivative of propionic acid with a 4-aminophenol group attached to the second carbon atom. This chemical is commonly used in the synthesis of pharmaceuticals and organic compounds due to its unique structure and properties. It is also utilized in the development of new drugs and as a building block for the creation of various organic compounds. Additionally, it has potential applications in the fields of medicine, biotechnology, and materials science due to its versatile nature and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 117011-70-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,0,1 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 117011-70:
(8*1)+(7*1)+(6*7)+(5*0)+(4*1)+(3*1)+(2*7)+(1*0)=78
78 % 10 = 8
So 117011-70-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO3/c1-10(2,9(12)13)14-8-5-3-7(11)4-6-8/h3-6H,11H2,1-2H3,(H,12,13)

117011-70-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-aminophenoxy)-2-methylpropanoic acid

1.2 Other means of identification

Product number -
Other names AB1105

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:117011-70-8 SDS

117011-70-8Relevant articles and documents

Design, synthesis and in vivo screening of some novel quinazoline analogs as anti-hyperlipidemic and hypoglycemic agents

Mokale, Santosh N.,Palkar, Akash D.,Dube, Pritam N.,Sakle, Nikhil S.,Miniyar, Pankaj B.

supporting information, p. 272 - 276 (2016/01/09)

A novel series of substituted quinazoline derivatives were designed, synthesized and evaluated for their hypolipidemic activity in cholesterol induced hyperlipidemic rats. In vivo screening concluded that compounds A-4, C-5 and C-6 have shown potent antihyperlipidemic activity by decreasing the plasma level of triglycerides (TG), very low density lipoprotein (VLDL), low density lipoprotein (LDL), followed by increase in level of high density lipoprotein (HDL).

Allosteric modifiers of hemoglobin useful for decreasing oxygen affinity and preserving oxygen carrying capability of stored blood

-

, (2008/06/13)

A family of compounds has been found to be useful for right-shifting hemoglobin towards a low oxygen affinity state. The compounds are capable of acting on hemoglobin in whole blood. In addition, the compounds can maintain the oxygen affinity in blood during storage and can restore the oxygen affinity of outdated blood.

Medical uses of allosteric hemoglobin modifier compounds in patient care

-

, (2008/06/13)

A family of compounds has been found to be useful for right-shifting hemoglobin towards a low oxygen affinity state. The effect has particular application in a wide variety of treatments including hypoxia, hypothermia, ischemia, stroke, ARDS, COPD, surgical blood loss, acute nonvolemic hemodilutions, wounds, diabetic ulcers, chronic leg ulcers, pressure sores, tissue transplants, and sepsis. The compounds are capable of acting on hemoglobin in whole blood.

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