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2,4-Cyclopentadiene-1-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114492-25-0 Structure
  • Basic information

    1. Product Name: 2,4-Cyclopentadiene-1-carbonitrile
    2. Synonyms:
    3. CAS NO:114492-25-0
    4. Molecular Formula: C6H5N
    5. Molecular Weight: 91.1124
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114492-25-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,4-Cyclopentadiene-1-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-Cyclopentadiene-1-carbonitrile(114492-25-0)
    11. EPA Substance Registry System: 2,4-Cyclopentadiene-1-carbonitrile(114492-25-0)
  • 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: 114492-25-0(Hazardous Substances Data)

114492-25-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114492-25-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,9 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114492-25:
(8*1)+(7*1)+(6*4)+(5*4)+(4*9)+(3*2)+(2*2)+(1*5)=110
110 % 10 = 0
So 114492-25-0 is a valid CAS Registry Number.

114492-25-0SDS

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 cyanocyclopentadiene

1.2 Other means of identification

Product number -
Other names Cyano-cyclopentadien

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:114492-25-0 SDS

114492-25-0Downstream Products

114492-25-0Relevant articles and documents

Homogenous Gas-Phase Formation and Destruction of Anthranil from o-Nitrotoluene Decomposition

He, Y. Z.,Cui, J. P.,Mallard, W. G.,Tsang, W.

, p. 3754 - 3759 (2007/10/02)

Dilute quantities of o-nitrotoluene and anthranil have been pyrolyzed in comparative rate single pulse shock tube experiments.Rather than C-NO2 bond cleavage and NO2 isomerization found as major channels in p-nitrotoluene decomposition, we demonstrate that the important pathway for pyrolysis involves the formation of anthranil with the following overall rate expression: k(o-nitrotoluene -> anthranil) = 1.2 x 1013 exp(-26020/T)/s.The anthranil that is formed is very unstable under our conditions; the rate expression for disappearence has been found to be the following: k(anthranil)d = 3.7 x 1015 exp(-25800/T)/s.Arguments are presented that suggest that the first rate expression is representative of a retroene reaction and the second expression is for the breaking of the N-O bond in anthranil.These conclusions emphasize the difference in results from shock tube and laser pyrolysis experiments.Their implications on the initiation reactions in the decomposition of nitroaromatic explosives are discussed.

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