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3332-38-5

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3332-38-5 Usage

Explanation

The molecular formula represents the number of carbon (C) and hydrogen (H) atoms in the compound, which is 16 carbon atoms and 16 hydrogen atoms in this case.
2. Hydrocarbon compound

Explanation

A hydrocarbon is an organic compound consisting entirely of hydrogen and carbon atoms. In this case, 1,3,5,7,9,11,13,15-Cyclohexadecaoctaene is a hydrocarbon with 16 carbon and 16 hydrogen atoms.
3. Highly unsaturated cyclic compound

Explanation

The term "highly unsaturated" refers to the presence of multiple double bonds (C=C) in the compound. The "cyclic" part indicates that the carbon atoms are arranged in a ring structure.
4. 16 carbon atoms in a ring structure

Explanation

The compound has a total of 16 carbon atoms, all connected in a closed ring, forming the backbone of the molecule.
5. Presence of multiple double bonds

Explanation

The compound has eight carbon-carbon double bonds (C=C), which contribute to its high degree of unsaturation and reactivity.
6. High reactivity

Explanation

Due to the presence of multiple double bonds, 1,3,5,7,9,11,13,15-Cyclohexadecaoctaene is highly reactive and prone to undergoing addition reactions with various reagents.
7. Used as a starting material in organic synthesis

Explanation

The compound's reactivity makes it a valuable starting material for the synthesis of a wide range of other organic compounds.
8. Can produce a wide range of compounds through chemical reactions

Explanation

The compound's versatility in undergoing various chemical reactions allows it to be transformed into a diverse array of other compounds, making it useful in organic chemistry.
9. Interest in the field of organic chemistry

Explanation

The unique structure and reactivity of 1,3,5,7,9,11,13,15-Cyclohexadecaoctaene make it an object of study and interest for researchers in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 3332-38-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,3 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3332-38:
(6*3)+(5*3)+(4*3)+(3*2)+(2*3)+(1*8)=65
65 % 10 = 5
So 3332-38-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H16/c1-2-4-6-8-10-12-14-16-15-13-11-9-7-5-3-1/h1-16H/b2-1-,3-1-,4-2-,5-3+,6-4+,7-5+,8-6+,9-7-,10-8-,11-9-,12-10-,13-11+,14-12+,15-13+,16-14+,16-15-

3332-38-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexadecaoctaene

1.2 Other means of identification

Product number -
Other names 1,3,5,7,9,11,13,15-Cyclohexadecaoctaene

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:3332-38-5 SDS

3332-38-5Relevant articles and documents

Isotopic Exchange Involving the Annulene Anion Radical and Its Dimerization to the Annulene Anion Radical

Stevenson, Cheryl D.,Burton, Richard D.,Peters, Steve J.,Reiter, Richard C.

, p. 5838 - 5842 (2007/10/02)

The addition of D2O to hexamethylphosphoramide solutions of the potassium salt of the annulene anion radical results in the slow (days) formation of the monodeuteriated anion radical (C8H7D1.1-).However, several days after a similar addition to the sodium salt solution, no C8H7D1.1- is present.Instead, the anion radical of annulene is found.These observations led to EPR and NMR studies, which have revealed the mechanism of each process.The mechanisms are based upon the facts that ion association is necessary for the isotope exchange reaction and the absence of ion association is required for the dimerization.Solutions of deuteriated annulene anion radical, annulene dianion, annulene anion radical, and annulene dianion can be readily generated from reduced solutions of annulene for EPR, NMR, etc. studies by making use of the isotopic exchange and dimerization mentioned above.

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