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1,3-Cyclopentadiene, 1,4-dimethyl- is a chemical compound with the molecular formula C7H10. It is a colorless liquid with a pungent odor and is classified as a conjugated diene due to the presence of two carbon-carbon double bonds separated by a single bond. 1,3-Cyclopentadiene, 1,4-dimethyl- is an important building block in organic synthesis, particularly for the production of various polymers and pharmaceuticals. It is also known as 1,4-dimethylcyclopentadiene or dimethylcyclopentadiene. The compound is insoluble in water but soluble in organic solvents. It is sensitive to light and heat, and therefore, it should be stored in a cool, dark place to prevent decomposition. Due to its reactivity, it is used in various chemical reactions, such as Diels-Alder reactions, which are crucial for the synthesis of complex organic molecules.

5602-47-1

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5602-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5602-47-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,0 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5602-47:
(6*5)+(5*6)+(4*0)+(3*2)+(2*4)+(1*7)=81
81 % 10 = 1
So 5602-47-1 is a valid CAS Registry Number.

5602-47-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dimethylcyclopenta-1,3-diene

1.2 Other means of identification

Product number -
Other names 1,3-Dimethyl-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:5602-47-1 SDS

5602-47-1Downstream Products

5602-47-1Relevant academic research and scientific papers

An Electron Spin Resonance Study of the Methylcyclopentadienyl Radicals, MenH5-nC5 (n=1-5)

Davies, Alwyn G.,Lusztyk, Ewa,Lusztyk, Janusz

, p. 729 - 736 (2007/10/02)

The radicals MenC5H5-n have been generated by photolysis of the corresponding hydrocarbons (n=3-5) or mercury derivatives (n=0-5) and their e.s.r. spectra have been recorded.The spectra are interpreted in terms of thermal population of the ψA and ψS molecular orbitals, for which the predicted hyperfine coupling constants are calculated by the McLachlan equation, taking λ 0.75 and Q(C5H5) -30 and Q(Me5C5) 31.85 G.The energy separations between the ψA and ψS MOs can be rationalised on the assumption that a methyl substituent on a carbon atom of the cyclopentadienyl carrying a unit ?-electron has a destablising interaction, within a factor of two, of 10 kJ mol-1.

Etude des transformations catalytiques sur alumine de β-tetrahydrofurylmethanols

Infarnet, Yves,Accary, Armand,Huet, Jean

, p. 261 - 266 (2007/10/02)

The products obtained by treatment of β-tetrahydrofurylmethanols at 310-330 deg C, using alumina as catalyst are studied.The nature of the products-furans, tetrahydrofurans, aliphatic and cyclic dienes-shows that beside the simple dehydration side reactions take place leading, as the case may be, to dehydrogenation, raduction, ring opening and fragmentation.

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