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124070-95-7

(1S,7aR)-1-(furan-3-yl)-4,4,7a-trimethyl-1,4,5,6,7,7a-hexahydro-2H-inden-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124070-95-7 Structure

  • Basic information

    1. Product Name: (1S,7aR)-1-(furan-3-yl)-4,4,7a-trimethyl-1,4,5,6,7,7a-hexahydro-2H-inden-2-one
    2. Synonyms:
    3. CAS NO:124070-95-7
    4. Molecular Formula: C16H20O2
    5. Molecular Weight: 244.3288
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124070-95-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 344.2°C at 760 mmHg
    3. Flash Point: 161.2°C
    4. Appearance: N/A
    5. Density: 1.09g/cm3
    6. Vapor Pressure: 6.7E-05mmHg at 25°C
    7. Refractive Index: 1.544
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (1S,7aR)-1-(furan-3-yl)-4,4,7a-trimethyl-1,4,5,6,7,7a-hexahydro-2H-inden-2-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: (1S,7aR)-1-(furan-3-yl)-4,4,7a-trimethyl-1,4,5,6,7,7a-hexahydro-2H-inden-2-one(124070-95-7)
    12. EPA Substance Registry System: (1S,7aR)-1-(furan-3-yl)-4,4,7a-trimethyl-1,4,5,6,7,7a-hexahydro-2H-inden-2-one(124070-95-7)

  • 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: 124070-95-7(Hazardous Substances Data)

124070-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124070-95-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,0,7 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 124070-95:
(8*1)+(7*2)+(6*4)+(5*0)+(4*7)+(3*0)+(2*9)+(1*5)=97
97 % 10 = 7
So 124070-95-7 is a valid CAS Registry Number.

124070-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (1RS,7aSR)-1-(3-furyl)-4,4,7a-trimethyl-1,4,5,6,7,7a-hexahydro-2H-inden-2-one

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:124070-95-7 SDS

124070-95-7Relevant articles and documents

Synthesis of Insert Antifeedants Related to Azadiradione

Mateos, A. Fernandez,Barba, A. Lopez,Coca, G. Pascual,Gonzalez, R. Rubio,Hernandez, C. Tapia

, p. 1381 - 1383 (2007/10/03)

An efficient synthesis of a model insect antifeedant based on the C, D and E rings of the limonoid azadiradione has been developed. (8 steps 18percent overall yield).The key steps were an electrocyclization induced by acids 4->5 and a dyotropic rearran

Model insect antifeedants. Synthesis of azadiradione fragments through acyl radicals cyclizations and stannane coupling reactions

Fernandez-Mateos, Alfonso,Coca, Gustavo Pascual,Gonzalez, Rosa Rubio,Hernandez, Carolina Tapia

, p. 4817 - 4828 (2007/10/03)

A diastereoselective and versatile synthesis of the model insect antifeedant 16 related to azadiradione has been achieved in nine steps starting from α-cyclocitral 1. The key steps involve intramolecular alkene addition of an acyl radical and a Stille coupling reaction of a vinyl iodide with a stannylfuran.

Stereoselective Addition of Enol Silanes to Nitro Olefins. A Simple Synthesis of Compounds Related to the Insect Antifeedants Azadiradion and Gedunin.

Mateos, A. Fernandez,Fuente Blanco, Jesus A. de la

, p. 1349 - 1354 (2007/10/02)

The Lewis acid mediated aldol reactions of 1-cyclohexene (2) and 2,6,6-trimethyl-1-cyclohexene (6) with (E)-1-(3-furyl)-2-nitro-1-propene (1) was investigated (Schemes I and II and Chart II).The addition of enol s

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