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7-methoxy-2,3-dihydro-1H-inden-1-amine, also known as Indan-1-amine, 7-methoxy-2,3-dihydro-, is an organic compound belonging to the aromatic homomonocyclic compounds. It features a unique structure with a benzene ring fused to a cyclopentane, which endows it with aromatic properties. Despite its distinctive structure, this compound has not been extensively studied, and its potential applications or properties beyond its basic chemical composition remain largely unexplored. 7-methoxy-2,3-dihydro-1H-inden-1-amine's molecular formula is C10H13NO.

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  • 1032279-33-6 Structure
  • Basic information

    1. Product Name: 7-methoxy-2,3-dihydro-1H-inden-1-amine
    2. Synonyms: 7-methoxy-2,3-dihydro-1H-inden-1-amine;2,3-dihydro-7-Methoxy-1H-inden-1-aMine
    3. CAS NO:1032279-33-6
    4. Molecular Formula: C10H13NO
    5. Molecular Weight: 163.21632
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1032279-33-6.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.: under inert gas (nitrogen or Argon) at 2–8 °C
    8. Solubility: N/A
    9. CAS DataBase Reference: 7-methoxy-2,3-dihydro-1H-inden-1-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-methoxy-2,3-dihydro-1H-inden-1-amine(1032279-33-6)
    11. EPA Substance Registry System: 7-methoxy-2,3-dihydro-1H-inden-1-amine(1032279-33-6)
  • 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: 1032279-33-6(Hazardous Substances Data)

1032279-33-6 Usage

Uses

Due to the limited information available on 7-methoxy-2,3-dihydro-1H-inden-1-amine, its specific applications are not well-documented. However, given its classification as an aromatic homomonocyclic compound, it may potentially be used in various chemical and pharmaceutical industries for the following purposes:
Used in Chemical Synthesis:
7-methoxy-2,3-dihydro-1H-inden-1-amine may be used as a building block or intermediate in the synthesis of more complex organic compounds, particularly those with aromatic structures.
Used in Pharmaceutical Industry:
Given its unique structure, 7-methoxy-2,3-dihydro-1H-inden-1-amine could potentially be used as a starting material or intermediate in the development of new pharmaceutical compounds, including drugs with novel therapeutic properties.
Used in Research and Development:
As a relatively unexplored compound, 7-methoxy-2,3-dihydro-1H-inden-1-amine may be utilized in research and development settings to study its chemical properties, reactivity, and potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1032279-33-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,2,7 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1032279-33:
(9*1)+(8*0)+(7*3)+(6*2)+(5*2)+(4*7)+(3*9)+(2*3)+(1*3)=116
116 % 10 = 6
So 1032279-33-6 is a valid CAS Registry Number.

1032279-33-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methoxy-2,3-dihydro-1H-inden-1-amine

1.2 Other means of identification

Product number -
Other names 7-methoxyindan-1-ylamine

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:1032279-33-6 SDS

1032279-33-6Downstream Products

1032279-33-6Relevant articles and documents

Synthesis and carbonic anhydrase inhibitory effects of novel sulfamides derived from 1-aminoindanes and anilines

Akbaba, Yusuf,Bastem, Enes,Topal, Fevzi,Gülin, Ilhami,Maras, Ahmet,G?ksu, Süleyman

, p. 950 - 957 (2014)

Three 1-aminoindanes, four anilines and BnOH or t-BuOH were reacted with chlorosulfonyl isocyanate to give sulfamoyl carbamates. Pd-C catalysed hydrogenolysis reactions of carbamates or deprotection of the Boc group of the carbamates with CF3CO2H afforded

6-SUBSTITUTED BENZOXAZINES

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Page/Page column 23, (2010/04/23)

The present invention is concerned with 6-substituted benzoxazine derivatives of formula (I) wherein X, Y, R1 and R2 are as described herein, their manufacture, and pharmaceutical compositions containing them. The active compounds of the present invention are 5-HT5A receptor antagonists, useful in the prevention and/or treatment of depression, anxiety disorders, schizophrenia, panic disorders, agoraphobia, social phobia, obsessive compulsive disorders, post-traumatic stress disorders, pain, memory disorders, dementia, disorders of eating behaviors, sexual dysfunction, sleep disorders, abuse of drugs, motor disorders, Parkinson's disease, psychiatric disorders or gastrointestinal disorders.

2-AMINOQUINOLINES

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Page/Page column 35, (2009/09/25)

The present invention is concerned with 2-aminoquinoline derivatives of formula I where R1, R2, R3, R4, R5, R6, A, and n are as defined in the specification and claims, their use 5-HT5

SUBSTITUTED FLUOROETHYL UREAS AS ALPHA 2 ADRENERGIC AGENTS

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Page/Page column 20, (2008/12/04)

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

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