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50438-50-1

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

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  • 50438-50-1 Structure

  • Basic information

    1. Product Name: 1-METHOXYCYCLOHEPTENE
    2. Synonyms: 1-METHOXYCYCLOHEPTENE
    3. CAS NO:50438-50-1
    4. Molecular Formula: C8H14O
    5. Molecular Weight: 126.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 50438-50-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 189.436°C at 760 mmHg
    3. Flash Point: 60.089°C
    4. Appearance: /
    5. Density: 0.891g/cm3
    6. Vapor Pressure: 0.788mmHg at 25°C
    7. Refractive Index: 1.456
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-METHOXYCYCLOHEPTENE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-METHOXYCYCLOHEPTENE(50438-50-1)
    12. EPA Substance Registry System: 1-METHOXYCYCLOHEPTENE(50438-50-1)

  • 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: 50438-50-1(Hazardous Substances Data)

50438-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50438-50-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,3 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 50438-50:
(7*5)+(6*0)+(5*4)+(4*3)+(3*8)+(2*5)+(1*0)=101
101 % 10 = 1
So 50438-50-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O/c1-9-8-6-4-2-3-5-7-8/h6H,2-5,7H2,1H3

50438-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methoxycycloheptene

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:50438-50-1 SDS

50438-50-1Relevant articles and documents

Ring Expansions via Photoinduced Single Electron Transfer Promoted Opening of Cyclopropyl Ethers

Gassman, Paul G.,Burns, Stephen J.

, p. 5576 - 5578 (2007/10/02)

A general method of ring expansion involving acetal to ring-homologated acetal is described.The key steps in the overall process involve (a) acetal to enol ether conversion, (b) cyclopropane formation, and (c) photoinduced single electron transfer promoted opening of the cyclopropane.

Photochemistry of Alkyl Halides. 10. Vinyl Halides and Vinylidene Dihalides

Kropp, Paul J.,McNeely, Steven A.,Davis, Robert Drummond

, p. 6907 - 6915 (2007/10/02)

The photobehavior of the acyclic vinyl iodide 2, the 1-iodocycloalkenes 11-14 and 39, the (halomethylene)cycloalkanes 45-48, and the (dihalomethylene)cyclohexanes 62-64 has been studied.Except for the dichloride 64, which exhibited only radical behavior, each of the halides afforded a mixture of ionic and radical products.The two bromides studied, 48 and 63, afforded lower ratios of ionic to radical products than the corresponding iodides 45 and 62.Irradiation of vinyl iodides was found to be a convenient and powerful method for the generation of vinyl cations, including the highly strained 1-cyclohexenyl and 1-cyclopentenyl cations and the unstabilized α-unsubstituted cations 51 and 54.The latter cations underwent rearrangement to the ring-expanded 1-cycloalkenyl cations 28 and 36, respectively.Lowering the temperature of the irradiation of iodides 13, 14, and 45 resulted in an increased ratio of ionic to radical products.However, iodide 47, which underwent principally fragmentation to enyne 61, showed little temperature effect.

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