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126489-69-8

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126489-69-8 Usage

Type of compound

Aromatic amine derivative

Structure

A propanediol molecule with an amino group attached to the aromatic ring

Applications

a. Synthesis of pharmaceuticals and organic compounds
b. Production of polyesters, polyurethanes, and epoxy resins
c. Reagent in organic synthesis
d. Intermediate in the production of dyes and pigments

Potential uses

a. Antioxidant
b. Anti-inflammatory agent
c. Pharmaceutical and nutraceutical industries

Molecular weight

166.22 g/mol

Appearance

Colorless to pale yellow liquid or solid

Solubility

Soluble in water, ethanol, and other polar solvents

Stability

Stable under normal temperature and pressure conditions

Reactivity

Reacts with oxidizing agents, acids, and bases

Hazards

May be harmful if swallowed, inhaled, or absorbed through the skin

Safety measures

Use appropriate personal protective equipment (PPE) and handle in a well-ventilated area

Storage

Store in a cool, dry, and well-ventilated area, away from incompatible substances and sources of ignition

Disposal

Dispose of in accordance with local, national, and international regulations for hazardous materials

Environmental impact

Potentially harmful to aquatic life and should be handled with care to prevent environmental contamination

Regulatory status

May be subject to specific regulations and restrictions depending on the region and intended use.

Check Digit Verification of cas no

The CAS Registry Mumber 126489-69-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,4,8 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 126489-69:
(8*1)+(7*2)+(6*6)+(5*4)+(4*8)+(3*9)+(2*6)+(1*9)=158
158 % 10 = 8
So 126489-69-8 is a valid CAS Registry Number.

126489-69-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-aminophenyl)propane-1,3-diol

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:126489-69-8 SDS

126489-69-8Relevant articles and documents

Reducing ion channel activity in a series of 4-heterocyclic arylamide FMS inhibitors

Wilson, Kenneth J.,Illig, Carl R.,Chen, Jinsheng,Wall, Mark J.,Ballentine, Shelley K.,Desjarlais, Renee L.,Chen, Yanmin,Schubert, Carsten,Donatelli, Robert,Petrounia, Ioanna,Crysler, Carl S.,Molloy, Christopher J.,Chaikin, Margery A.,Manthey, Carl L.,Player, Mark R.,Tomczuk, Bruce E.,Meegalla, Sanath K.

scheme or table, p. 3925 - 3929 (2010/09/03)

During efforts to improve the bioavailability of FMS kinase inhibitors 1 and 2, a series of saturated and aromatic 4-heterocycles of reduced basicity were prepared and evaluated in an attempt to also improve the cardiovascular safety profile over lead ary

Design and synthesis of benzoic acid derivatives as influenza neuraminidase inhibitors using structure-based drug design

Chand, Pooran,Babu, Yarlagadda S.,Bantia, Shanta,Chu, Naiming,Cole, L. Brent,Kotian, Pravin L.,Laver, W. Graeme,Montgomery, John A.,Pathak, Ved P.,Petty, Sandra L.,Shrout, David P.,Walsh, David A.,Walsh, Gerald M.

, p. 4030 - 4052 (2007/10/03)

A series of 94 benzoic acid derivatives was synthesized and tested for its ability to inhibit influenza neuraminidase. The enzyme-inhibitor complex structure was determined by X-ray crystallographic analysis for compounds which inhibited the enzyme. The most potent compound tested in vitro, 5 (4- (acetylamino)-3-guanidinobenzoic acid), had an IC50 = 2.5 x 10-6 M against N9 neuraminidase. Compound 5 was oriented in the active site of the neuraminidase in a manner that was not predicted from the reported active site binding of GANA (4) with neuraminidase. In a mouse model of influenza, 5 did not protect the mice from weight loss due to the influenza virus when dosed intranasally.

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