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320574-77-4

6-Hydroxy-7-allylindan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 320574-77-4 Structure

  • Basic information

    1. Product Name: 6-Hydroxy-7-allylindan-1-one
    2. Synonyms: 6-Hydroxy-7-allylindan-1-one
    3. CAS NO:320574-77-4
    4. Molecular Formula: C12H12O2
    5. Molecular Weight: 188.22248
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 320574-77-4.mol

  • Chemical Properties

    1. Melting Point: 123～125℃
    2. Boiling Point: 364.5±41.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.192±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 9.79±0.20(Predicted)
    10. CAS DataBase Reference: 6-Hydroxy-7-allylindan-1-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-Hydroxy-7-allylindan-1-one(320574-77-4)
    12. EPA Substance Registry System: 6-Hydroxy-7-allylindan-1-one(320574-77-4)

  • 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: 320574-77-4(Hazardous Substances Data)

320574-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 320574-77-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,0,5,7 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 320574-77:
(8*3)+(7*2)+(6*0)+(5*5)+(4*7)+(3*4)+(2*7)+(1*7)=124
124 % 10 = 4
So 320574-77-4 is a valid CAS Registry Number.

320574-77-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-hydroxy-7-prop-2-enyl-2,3-dihydroinden-1-one

1.2 Other means of identification

Product number -
Other names 6-Hydroxy-7-allylindan-1-one

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:320574-77-4 SDS

320574-77-4Upstream product

320574-77-4Downstream Products

320574-77-4Relevant articles and documents

PROCESS FOR PREPARING 1,2,6,7-TETRAHYDRO-8H-INDENO[5,4-B]FURAN-8-ONE

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Page/Page column 11, (2011/05/05)

The invention provides a process for preparing 1,2,6,7-tetrahydro-8H-indeno-[5,4-b]furan-8-one (I), said process comprising the steps: (i) subjecting 6-hydroxy-7-allyl-indan-1-one to ozonolysis followed by reduction in the presence of methanol to form 2-methoxy-1,2,6,7-tetrahydro-8H-indeno[5,4-b]furan-8-one; (ii) subjecting 6-hydroxy-7-allyl-indan-1-one to alcohol elimination to form 6,7-dihydro-8H-indeno-[5,4-b]furan-8-one; and (iii) subjecting 6,7-dihydro-8H-indeno-[5,4-b]furan-8-one to hydrogenation to obtain 1,2,6,7-tetrahydro-8H-indeno[5,4-b]furan-8-one.

PROCESS FOR THE PREPARATION OF RAMELTEON

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Page/Page column 3; 8-9, (2010/09/18)

A process is described for the preparation on an industrial scale of N-[2-(8S)-1,6,7,8-tetrahydro-2H-indeno[5,4-b]furan-8-yl]ethyl]propionamide, ramelteon, having the structure illustrated below:

PROCESS FOR THE PREPARATION OF RAMELTEON

-

Page/Page column 17-18, (2010/10/03)

A process is described for the preparation on an industrial scale of N-[2-(8S)- 1,6,7,8-tetrahydro-2H-indeno[5,4-b]furan-8-yl] propionamide, ramelteon, having the structure illustrated below: (I).

Predicting the Claisen rearrangement regioselectivity of allylindanyl and allyltetrahydronaphthalenyl ether derivatives by 1H NMR experiments

Rodrigues, Denise C.,Fernandes, Sergio A.,Marsaioli, Anita J.

, p. 970 - 974 (2007/10/03)

The regioselectivity of the Claisen rearrangement of allylindanyl and allyltetrahydronaphthalenyl ether derivatives can be predicted by conformational preference detected by 1H NMR NOE difference spectra and T1 measurements. Copyright

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