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34511-01-8

3,4-Octadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 34511-01-8 Structure

  • Basic information

    1. Product Name: 3,4-Octadiene
    2. Synonyms: 3,4-Octadiene
    3. CAS NO:34511-01-8
    4. Molecular Formula: C8H14
    5. Molecular Weight: 110.1968
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 34511-01-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 128.3°Cat760mmHg
    3. Flash Point: 17.5°C
    4. Appearance: /
    5. Density: 0.72g/cm3
    6. Vapor Pressure: 13mmHg at 25°C
    7. Refractive Index: 1.425
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3,4-Octadiene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3,4-Octadiene(34511-01-8)
    12. EPA Substance Registry System: 3,4-Octadiene(34511-01-8)

  • 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: 34511-01-8(Hazardous Substances Data)

34511-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34511-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,1 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34511-01:
(7*3)+(6*4)+(5*5)+(4*1)+(3*1)+(2*0)+(1*1)=78
78 % 10 = 8
So 34511-01-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H14/c1-3-5-7-8-6-4-2/h5,8H,3-4,6H2,1-2H3

34511-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name octa-3,4-diene

1.2 Other means of identification

Product number -
Other names 3,4-octadiene

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:34511-01-8 SDS

34511-01-8Downstream Products

34511-01-8Relevant articles and documents

REACTIONS OF 3-ALKYL- AND 3,3-DIALKYL-1-BROMOALLENES WITH ORGANOCUPRATES: EFFECTS OF THE NATURE OF THE CUPRATE REAGENT ON THE REGIO- AND STEREOSELECTIVITY

Caporusso, Anna Maria,Polizzi, Carmela,Lardicci, Luciano

, p. 6073 - 6076 (2007/10/02)

Organocuprates induce 1,3- and direct substitution in 3-alkyl- and 3,3-dialkyl-1-bromo-1,2-dienes leading respectively to either terminal acetylenes or allenic hydrocarbons.The nature of the cuprate exerts a prominent role in determining both the regio- and the stereochemistry of these reactions.

HOMOALLENYL RADICALS

Crandall, J. K.,Tindell, G. L.,Manmade, A.

, p. 3769 - 3772 (2007/10/02)

Several homoallenyl radicals have been generated by the reaction of the corresponding iodides with Bu3SnH and found to produce small amounts of vinylcyclopropanes in addition to allene hydrocarbons establishing that homoallenyl radicals cyclize to isomeri

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