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CAS

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17190-90-8

2-Methoxynorbornene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 17190-90-8 Structure

  • Basic information

    1. Product Name: 2-Methoxynorbornene
    2. Synonyms: 2-Methoxynorbornene
    3. CAS NO:17190-90-8
    4. Molecular Formula: C8H12 O
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17190-90-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 188.2°C at 760 mmHg
    3. Flash Point: 59.3°C
    4. Appearance: /
    5. Density: 1g/cm3
    6. Vapor Pressure: 0.835mmHg at 25°C
    7. Refractive Index: 1.498
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-Methoxynorbornene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Methoxynorbornene(17190-90-8)
    12. EPA Substance Registry System: 2-Methoxynorbornene(17190-90-8)

  • 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: 17190-90-8(Hazardous Substances Data)

17190-90-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17190-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,9 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17190-90:
(7*1)+(6*7)+(5*1)+(4*9)+(3*0)+(2*9)+(1*0)=108
108 % 10 = 8
So 17190-90-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O/c1-9-8-5-6-2-3-7(8)4-6/h5-7H,2-4H2,1H3

17190-90-8SDS

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 3-methoxybicyclo[2.2.1]hept-2-ene

1.2 Other means of identification

Product number -
Other names 2-methoxynorbornene

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:17190-90-8 SDS

17190-90-8Relevant articles and documents

Synthesis of Cyclic and Acyclic Enol Ethers (Vinyl Ethers)

Gassman, Paul G.,Burns, Stephen J.,Pfister, Keith B.

, p. 1449 - 1457 (2007/10/02)

A general method has been developed for the conversion of both cyclic and acyclic acetals of cyclic ketones, acyclic ketones, and aldehydes into enol ethers through treatment of the acetal with trimethylsilyl triflate in the presence of N,N-diisopropylethylamine.The range of isolated yields of enol ethers from the various classes of acetals was as follows: cyclic acetals of cyclic ketones, 83-98percent; acyclic acetals of ketones, 72-94percent; acyclic and cyclic acetals of aldehydes, 65-90percent.

Copper catalysed preparation of vinyl ethers from unactivated vinylic halides

Keegstra

, p. 2681 - 2690 (2007/10/02)

Vinylic halides have been treated with sodium methoxide in the presence of 10 mol% of copper bromide. Most of the vinylic methyl ethers could thus be obtained in a good yield. The reaction proceeds with a 100% retention of configuration. The mechanism of

ORGANIC TRANSFORMATIONS VIA METAL SILANE REAGENTS: SYNTHESES OF VINYL ETHERS FROM DIMETHYL KETALS AND (CO)5MnSi(CH3)3

Marsi, Marianne,Gladysz, J. A.

, p. 631 - 634 (2007/10/02)

The reaction of dimethyl ketals wit (CO)5MnSi(CH3)3 (1) at 50 deg C in CH3CN affords methyl enol ethers, generally in 75-95percent yields.

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