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tricyclo[3.1.0.0~2,6~]hex-3-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 659-85-8 Structure
  • Basic information

    1. Product Name: tricyclo[3.1.0.0~2,6~]hex-3-ene
    2. Synonyms: Tricyclo[3.1.0.0~2,6~]hex-3-ene
    3. CAS NO:659-85-8
    4. Molecular Formula: C6H6
    5. Molecular Weight: 78.1118
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 659-85-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 77.6°C at 760 mmHg
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.264g/cm3
    6. Vapor Pressure: 106mmHg at 25°C
    7. Refractive Index: 1.681
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: tricyclo[3.1.0.0~2,6~]hex-3-ene(CAS DataBase Reference)
    11. NIST Chemistry Reference: tricyclo[3.1.0.0~2,6~]hex-3-ene(659-85-8)
    12. EPA Substance Registry System: tricyclo[3.1.0.0~2,6~]hex-3-ene(659-85-8)
  • 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: 659-85-8(Hazardous Substances Data)

659-85-8 Usage

Definition

benzvalene: A valence isomer ofbenzene, C6H6, with a bridged structure.

Check Digit Verification of cas no

The CAS Registry Mumber 659-85-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,5 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 659-85:
(5*6)+(4*5)+(3*9)+(2*8)+(1*5)=98
98 % 10 = 8
So 659-85-8 is a valid CAS Registry Number.

659-85-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzvalene

1.2 Other means of identification

Product number -
Other names Tricyclo<2.1.1.05,6>hex-2-en = Benzvalen

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:659-85-8 SDS

659-85-8Relevant articles and documents

LASER FLASH PHOTOLYSIS OF BENZENE - 6. PHOTOLYSIS IN AQUEOUS SOLUTION.

Shimo,Nakashima,Yoshihara

, p. 389 - 391 (1983)

Three transient absorption spectra in aqueous solution were observed by irradiation of benzene with an excimer laser (KrF, 248 nm or ArF, 193 nm). A short-lived absorption with a peak at 275 nm is assigned to the S//n implied by S//1 absorption. A long-lived absorption, which appears as a clear shoulder at 230 nm, stays longer than 500 ns and is not shortened by oxygen. This species is tentatively assigned to benzvalene, and the quantum yield is determined to be ca. 0. 1. Solvated electron with a peak at 720 nm was formed via multiphoton process at a power level of 60 mJ/cm**2 of an ArF laser.

Matrix-Controlled Photochemistry of Benzene and Pyridine

Johnstone, Duncan E.,Sodeau, John R.

, p. 165 - 169 (2007/10/02)

Dewar benzene has been shown to be a primary product from the photolysis of benzene in low temperature argon matrices at 253.7 nm.This is the first observation of Dewar benzene production at this wavelength and a mechanism is proposed that involves benzene S1-S2 state mixing induced by the matrix environment.Analogous experiments on the photolysis of pyridine show that the only primary products are isomeric species derived at least in part from a triplet state of pyridine, probably T1.This is the first observation of photochemistry from the T1 state and may be the process responsible for the small values of τp and ψp in pyridine.Analysis of the IR spectral bands points to the main product being Dewar pyridine although other isomers cannot be ruled out.In contrast to the gas phase, no decomposition of pyridine was found in matrices poducing compounds such as acrylonitrile, ethyne, and hydrogen cyanide.

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