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(R)-4-Methoxy-2,3-dihydro-1H-inden-1-aMine hydrochloride is a chiral amine chemical compound that belongs to the class of amines. It is characterized by its non-superimposable mirror image and is commonly used as a reagent in organic synthesis and pharmaceutical research. (R)-4-Methoxy-2,3-dihydro-1H-inden-1-aMine hydrochloride is often utilized in the production of pharmaceuticals and agrochemicals due to its ability to serve as a building block for more complex chemical structures. Additionally, it has potential therapeutic applications in the treatment of neurological disorders, owing to its interaction with the serotonin receptor. However, it is important to handle (R)-4-Methoxy-2,3-dihydro-1H-inden-1-aMine hydrochloride with care, as it can be toxic if ingested or inhaled.

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  • 1217445-49-2 Structure
  • Basic information

    1. Product Name: (R)-4-Methoxy-2,3-dihydro-1H-inden-1-aMine hydrochloride
    2. Synonyms: (R)-4-Methoxy-2,3-dihydro-1H-inden-1-aMine hydrochloride
    3. CAS NO:1217445-49-2
    4. Molecular Formula:
    5. Molecular Weight: 163.219
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1217445-49-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-4-Methoxy-2,3-dihydro-1H-inden-1-aMine hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-4-Methoxy-2,3-dihydro-1H-inden-1-aMine hydrochloride(1217445-49-2)
    11. EPA Substance Registry System: (R)-4-Methoxy-2,3-dihydro-1H-inden-1-aMine hydrochloride(1217445-49-2)
  • 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: 1217445-49-2(Hazardous Substances Data)

1217445-49-2 Usage

Uses

Used in Pharmaceutical Research and Organic Synthesis:
(R)-4-Methoxy-2,3-dihydro-1H-inden-1-aMine hydrochloride is used as a reagent in pharmaceutical research and organic synthesis for its ability to serve as a building block for more complex chemical structures.
Used in the Production of Pharmaceuticals:
(R)-4-Methoxy-2,3-dihydro-1H-inden-1-aMine hydrochloride is used as a key intermediate in the production of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in the Production of Agrochemicals:
(R)-4-Methoxy-2,3-dihydro-1H-inden-1-aMine hydrochloride is used as a building block in the production of agrochemicals, aiding in the development of new pesticides and other agricultural chemicals.
Used in the Treatment of Neurological Disorders:
(R)-4-Methoxy-2,3-dihydro-1H-inden-1-aMine hydrochloride is used as a potential therapeutic agent in the treatment of neurological disorders, due to its interaction with the serotonin receptor, which may help in managing various neurological conditions.
Used in Chemical Research:
(R)-4-Methoxy-2,3-dihydro-1H-inden-1-aMine hydrochloride is used as a subject of study in chemical research to explore its properties, reactivity, and potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1217445-49-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,4,4 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1217445-49:
(9*1)+(8*2)+(7*1)+(6*7)+(5*4)+(4*4)+(3*5)+(2*4)+(1*9)=142
142 % 10 = 2
So 1217445-49-2 is a valid CAS Registry Number.

1217445-49-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R)-4-methoxy-2,3-dihydro-1H-inden-1-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names (1r)-4-methoxyindanylamine hydrochloride

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:1217445-49-2 SDS

1217445-49-2Downstream Products

1217445-49-2Relevant articles and documents

Microwave-accelerated reductive amination between ketones and ammonium acetate

Dong, Li,Aleem, Saadat,Fink, Cynthia A.

experimental part, p. 5210 - 5212 (2010/11/05)

A new procedure for reductive amination between ketones and ammonium acetate has been developed to access a variety of primary amines. This protocol takes advantage of microwave heating to significantly accelerate the reaction and offers a convenient and effective method to access some interesting amines. This new procedure compares favorably to previously reported approaches in terms of practicality, efficiency, and functional group compatibility.

PYRIDINONE ANTAGONISTS OF ALPHA-4 INTEGRINS

-

, (2010/11/17)

The present invention provides compounds that are alpha4 integrin antagonists having a structure according to the following formula (I) or a tautomer, mixture of tautomers, salt or solvate thereof, wherein Cy, ring A, m, n, p, R1, R2

SUBSTITUTED FLUOROETHYL UREAS AS ALPHA 2 ADRENERGIC AGENTS

-

Page/Page column 16; 17, (2008/12/04)

Therapeutic compounds, and methods, compositions, and medicaments related thereto are disclosed herein.

Multicyclic bis-amide MMP inhibitors

-

Page/Page column 114, (2008/06/13)

The present invention relates generally to bis-amide group containing pharmaceutical agents, and in particular, to multicyclic bis-amide MMP-13 inhibitor compounds. More particularly, the present invention provides a new class of MMP-13 inhibiting compounds, containing a pyrimidinyl bis-amide group in combination with a heterocyclic moiety, that exhibit an increased potency and solubility in relation to currently known bis-amide group containing MMP-13 inhibitors.

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