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9003-73-0

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9003-73-0 Usage

General Description

POLYDIPENTENE is a polymer compound derived from the polymerization of dicyclopentadiene. It is a type of thermoplastic that is known for its high chemical resistance, low water absorption, and excellent electrical insulation properties. POLYDIPENTENE is commonly used in the production of various industrial and consumer products, including packaging materials, pipes, automotive components, and electrical insulation coatings. It is also known for its high optical clarity and resistance to heat, making it a popular choice for applications requiring transparent and durable materials. Overall, POLYDIPENTENE is a versatile and versatile chemical compound with a wide range of industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 9003-73-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 9,0,0 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 9003-73:
(6*9)+(5*0)+(4*0)+(3*3)+(2*7)+(1*3)=80
80 % 10 = 0
So 9003-73-0 is a valid CAS Registry Number.

9003-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Isopropenyl-1-methylcyclohexene

1.2 Other means of identification

Product number -
Other names -

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:9003-73-0 SDS

9003-73-0Relevant articles and documents

Ring-Opening Reactions of α- And β-Pinenes in Pressurized Hot Water in the Absence of Any Additive

Kawahara, Tomomi,Henmi, Yui,Onda, Natsu,Sato, Toshiyuki,Kawai-Nakamura, Akiko,Sue, Kiwamu,Iwamura, Hiizu,Hiaki, Toshihiko

, p. 1485 - 1491 (2013)

Reactions of α- and β-pinenes in pressurized hot water were examined in a batch reactor made of a SS316 1/2-in. tube at temperatures of 250-400 C, pressures of 4-30 MPa, and reaction times of 1-30 min in the absence of any additive under an argon atmosphere. The maximum yields of limonene from α-pinene were ca. 70% in 20 min at 300 C or 1 min at 400 C. Limonene was obtained from β-pinene in ca. 16% yield for 30 min at 300 C and 1 min at 400 C. Reversible production of myrcene in 14% yield and formation of unidentified C20 dimer fractions were noted for 1 min at 370 C from β-pinene. The conversion of α-pinene to limonene took place under anhydrous conditions, albeit at slightly lower yield of 65% compared to processes conducted in the presence of water, where increased limonene yield of 70% was observed for 1 min at 400 C. The conversion of β-pinene to limonene under anhydrous conditions was limited to 6.1% in contrast to 11.9% in the presence of water for 7 min at 370 C. In the presence of oxygen, p-cymene was formed in 23% and 24% yield at the expense of limonene from α- and β-pinenes, respectively, for 30 min at 400 C.

Method and Means for Releasing a Terpene Mixture to a Cannabis Flower During Storage

-

, (2021/09/17)

A method and means for releasing a terpene mixture to a Cannabis flower during storage with may be from a cotton pulp card or a two-way humidity pack with an additional terpene blend for keeping a Cannabis flower fresh while naturally increasing the desired terpene levels. The product is a blend of humidity regulating agents infused with terpenes (plant derived) which allows for the product to be paired with herbal material to increase and maintain the relative humidity, while transferring the flavor/aroma/taste terpenes from the package into the herbal material. There are two embodiments, the first is a Terp Pack+Humidity (“Terp Pack+RH”) which contains a herban material to increase and maintain relative humidity, while releasing the infused terenes, and the second is more simply a Terp Pack (“Terp Pack”) which contains no humidity enhancing material and is only a carrier for releasing the terpene mixture.

Nickel-catalyzed reductive deoxygenation of diverse C-O bond-bearing functional groups

Cook, Adam,MacLean, Haydn,St. Onge, Piers,Newman, Stephen G.

, p. 13337 - 13347 (2021/11/20)

We report a catalytic method for the direct deoxygenation of various C-O bond-containing functional groups. Using a Ni(II) pre-catalyst and silane reducing agent, alcohols, epoxides, and ethers are reduced to the corresponding alkane. Unsaturated species including aldehydes and ketones are also deoxygenated via initial formation of an intermediate silylated alcohol. The reaction is chemoselective for C(sp3)-O bonds, leaving amines, anilines, aryl ethers, alkenes, and nitrogen-containing heterocycles untouched. Applications toward catalytic deuteration, benzyl ether deprotection, and the valorization of biomass-derived feedstocks demonstrate some of the practical aspects of this methodology.

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