1002-33-1 Usage
Description
1,3-Octadiene, a colorless, flammable liquid with a strong, unpleasant odor, is a chemical compound with the formula C8H14. Classified as an alpha-omega diene, it is a versatile organic compound used in various industrial applications.
Uses
Used in Chemical Synthesis:
1,3-Octadiene is used as a monomer for the production of synthetic rubber, as it can be polymerized to form elastomers with properties similar to natural rubber. This makes it a valuable component in the manufacturing of various rubber products.
Used in Plastics and Resins Production:
1,3-Octadiene is used as a monomer in the production of plastics and resins, contributing to the creation of materials with specific properties required for different applications.
Used in Organic Compounds Synthesis:
1,3-Octadiene is utilized in the synthesis of various organic compounds, showcasing its importance in the chemical industry for creating a wide range of products.
Used as a Solvent in Industrial Processes:
Due to its solvent properties, 1,3-Octadiene is employed in industrial processes, aiding in the manufacturing and processing of certain materials.
However, it is important to note that 1,3-Octadiene is considered hazardous and should be handled with care due to its flammability and potential health risks if inhaled or ingested. Proper safety measures must be taken during its use to mitigate any associated risks.
Check Digit Verification of cas no
The CAS Registry Mumber 1002-33-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1002-33:
(6*1)+(5*0)+(4*0)+(3*2)+(2*3)+(1*3)=21
21 % 10 = 1
So 1002-33-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H14/c1-3-5-7-8-6-4-2/h3,5,7H,1,4,6,8H2,2H3
1002-33-1Relevant articles and documents
Synthesis and pyrolysis of two flavor precursors of oct-1-en-3-yl methylpyrazinecarboxylates
Lai, Miao,Ji, Xiaoming,Tao, Tao,Shan, Yuanyuan,Liu, Pengfei,Zhao, Mingqin
, p. 1627 - 1638 (2017)
To rich flavor additive species of pyrazines, two new compounds of 3,6-dimethyl-2,5-pyrazinedicarboxylic acid 1-octen-3-yl ester (DMPOE) and 3,5,6-trimethyl-2-pyrazinecarboxylic acid 1-octen-3-yl ester (TMPOE) were synthesized by KMnO4 oxidatio
Palladium-catalyzed preparation of dialkyl allylphosphonates. A new preparation of diethyl 2-oxoethylphosphonate
Malet,Moreno-Manas,Pleixats
, p. 2219 - 2228 (2007/10/02)
Palladium-catalyzed Michaelis-Arbuzov reaction of allyl acetates with trialkyl phosphites affords dialkyl allylphosphonates. Diethyl 2-oxoethylphosphonate is efficiently prepared by ozonization of diethyl allylphosphonate.
METAL COMPLEXES IN ORGANIC SYNTHESIS. VIII. ALLYLIC ALCOHOLS AS STARTING MATERIALS IN PALLADIUM-CATALYZED WITTIG-TYPE OLEFINIZATIONS.
Moreno-Manas,Truis
, p. 2154 - 2158 (2007/10/02)
Allylic alcohols, aldehydes, and triphenylphosphine participate in a one-pot process catalyzed by palladium, which is formally equivalent to the Wittig olefinization. It can be applied to both aliphatic and aromatic aldehydes. The resulting olefins which appear as mixtures of stereoisomers were fully hydrogenated. Two different mechanisms can account for the observed results.