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TERT-BUTYL [4-(2-AMINO-ETHYL)-PHENOXY]-ACETATE is a chemical compound with the molecular formula C15H23NO3. It is an ester derivative of 4-(2-amino-ethyl)-phenoxyacetic acid, known for its potential as a drug intermediate and pharmacological properties. TERT-BUTYL [4-(2-AMINO-ETHYL)-PHENOXY]-ACETATE is commonly used in the pharmaceutical and agrochemical industries and serves as a building block in the synthesis of various organic compounds. Due to its potentially hazardous properties, careful handling and storage are required.

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  • 124499-19-0 Structure
  • Basic information

    1. Product Name: TERT-BUTYL [4-(2-AMINO-ETHYL)-PHENOXY]-ACETATE
    2. Synonyms: TERT-BUTYL [4-(2-AMINO-ETHYL)-PHENOXY]-ACETATE;tert-butyl2-(4-(2-aminoethyl)phenoxy)acetate
    3. CAS NO:124499-19-0
    4. Molecular Formula: C14H21NO3
    5. Molecular Weight: 251.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124499-19-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 354.0±22.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.064±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 9.94±0.10(Predicted)
    10. CAS DataBase Reference: TERT-BUTYL [4-(2-AMINO-ETHYL)-PHENOXY]-ACETATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: TERT-BUTYL [4-(2-AMINO-ETHYL)-PHENOXY]-ACETATE(124499-19-0)
    12. EPA Substance Registry System: TERT-BUTYL [4-(2-AMINO-ETHYL)-PHENOXY]-ACETATE(124499-19-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 124499-19-0(Hazardous Substances Data)

124499-19-0 Usage

Uses

Used in Pharmaceutical Industry:
TERT-BUTYL [4-(2-AMINO-ETHYL)-PHENOXY]-ACETATE is used as a drug intermediate for its potential pharmacological properties. It plays a crucial role in the development of new medications, contributing to the advancement of healthcare and treatment options.
Used in Agrochemical Industry:
In the agrochemical industry, TERT-BUTYL [4-(2-AMINO-ETHYL)-PHENOXY]-ACETATE is utilized for its potential applications in the development of agrochemical products. Its use in this sector can contribute to the enhancement of crop protection and agricultural productivity.
Used in Organic Synthesis:
TERT-BUTYL [4-(2-AMINO-ETHYL)-PHENOXY]-ACETATE serves as a building block in the synthesis of various organic compounds. Its versatility in chemical reactions allows for the creation of a wide range of products, further expanding its applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 124499-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,9 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124499-19:
(8*1)+(7*2)+(6*4)+(5*4)+(4*9)+(3*9)+(2*1)+(1*9)=140
140 % 10 = 0
So 124499-19-0 is a valid CAS Registry Number.

124499-19-0SDS

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 tert-butyl 2-[4-(2-aminoethyl)phenoxy]acetate

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:124499-19-0 SDS

124499-19-0Relevant articles and documents

An Fc–Small Molecule Conjugate for Targeted Inhibition of the Adenosine 2A Receptor

Hsiao, Po-Yuan,Kalin, Jay H.,Sun, Im-Hong,Amin, Mohammed N.,Lo, Ying-Chun,Chiang, Meng-Jung,Giddens, John,Sysa-Shah, Polina,Gabrielson, Kathleen,Wang, Lai-Xi,Powell, Jonathan D.,Cole, Philip A.

, p. 1951 - 1960 (2016)

The adenosine A2A receptor (A2AR) is expressed in immune cells, as well as brain and heart tissue, and has been intensively studied as a therapeutic target for multiple disease indications. Inhibitors of the A2AR have the

2-(Arylalkylamino)adenosin-5'-uronamides: A New Class of Highly Selective Adenosine A2 Receptor Ligands

Hutchison, Alan J.,Williams, Michael,Jesus, Reynalda, de,Yokoyama, Rina,Oei, Howard H.,et al.

, p. 1919 - 1924 (2007/10/02)

The synthesis and receptor-binding profiles at adenosine receptor subtypes for a series of 2-(arylalkylamino)adenosin-5'-uronamides is described.Halogenated 2-phenethylamino analogues such as 3e show greater than 200-fold selectivity for the A2 receptor s

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