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(1S)-1-(2,4-DIMETHOXYPHENYL)ETHANAMINE is a phenethylamine derivative, an amine compound with a molecular formula of C10H15NO2 and a molecular weight of 181.23 g/mol. It is a chiral molecule with the (1S) configuration and features a 2,4-dimethoxyphenyl group attached to an ethanamine moiety. (1S)-1-(2,4-DIMETHOXYPHENYL)ETHANAMINE is of interest in the pharmaceutical and chemical industries due to its potential applications and properties.

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  • 1212264-50-0 Structure
  • Basic information

    1. Product Name: (1S)-1-(2,4-DIMETHOXYPHENYL)ETHANAMINE
    2. Synonyms: (1S)-1-(2,4-DIMETHOXYPHENYL)ETHANAMINE
    3. CAS NO:1212264-50-0
    4. Molecular Formula: C10H15NO2
    5. Molecular Weight: 181.2316
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1212264-50-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (1S)-1-(2,4-DIMETHOXYPHENYL)ETHANAMINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S)-1-(2,4-DIMETHOXYPHENYL)ETHANAMINE(1212264-50-0)
    11. EPA Substance Registry System: (1S)-1-(2,4-DIMETHOXYPHENYL)ETHANAMINE(1212264-50-0)
  • 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: 1212264-50-0(Hazardous Substances Data)

1212264-50-0 Usage

Uses

Used in Pharmaceutical Industry:
(1S)-1-(2,4-DIMETHOXYPHENYL)ETHANAMINE is used as a building block for the synthesis of various organic compounds and has potential applications in the development of new drugs and therapies. Its unique structure and chirality may contribute to its biological activities, making it a valuable compound for research and drug discovery.
Used in Chemical Research:
(1S)-1-(2,4-DIMETHOXYPHENYL)ETHANAMINE is used as a research compound to study its properties, reactivity, and potential applications in chemical synthesis. Its isomers with different stereochemistry may exhibit variations in their pharmacological properties, providing opportunities for the development of novel compounds with specific therapeutic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 1212264-50-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,2,2,6 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1212264-50:
(9*1)+(8*2)+(7*1)+(6*2)+(5*2)+(4*6)+(3*4)+(2*5)+(1*0)=100
100 % 10 = 0
So 1212264-50-0 is a valid CAS Registry Number.

1212264-50-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S)-1-(2,4-dimethoxyphenyl)ethanamine

1.2 Other means of identification

Product number -
Other names (S)-1-(2,4-Dimethoxyphenyl)ethanamine

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:1212264-50-0 SDS

1212264-50-0Relevant articles and documents

Chemoenzymatic synthesis and application of a new, easily chiral auxiliary for the synthesis of peptidomimetics via an Ugi reaction

Klossowski, Szymon,Brodzka, Anna,Zysk, Ma?gorzata,Ostaszewski, Ryszard

, p. 435 - 442 (2014/04/17)

A new chiral auxiliary derived from α-phenylethylamine, α-(2,4-dimethoxyphenyl)ethylamine is presented. It significantly expands upon the application of α-phenylethylamine derivatives used as chiral auxiliaries. A straightforward, chemoenzymatic synthesis

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