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3-METHYL-1,4-PENTADIENE is a colorless liquid chemical compound with a distinctive sweet odor, belonging to the class of pentadienes. It is primarily used as an intermediate in the synthesis of various chemical products, including pesticides, pharmaceuticals, and polymers.

1115-08-8

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1115-08-8 Usage

Uses

Used in Chemical Synthesis:
3-METHYL-1,4-PENTADIENE is used as an intermediate in the synthesis of various chemical products for its versatile reactivity and ability to form a wide range of compounds.
Used in Pharmaceutical Industry:
3-METHYL-1,4-PENTADIENE is used as a monomer in the production of synthetic elastomers and resins, which are essential components in the manufacturing of certain pharmaceutical products.
Used in Pesticide Industry:
3-METHYL-1,4-PENTADIENE is used as a monomer in the production of synthetic elastomers and resins, which are utilized in the formulation of some pesticides.
Used in Polymer Industry:
3-METHYL-1,4-PENTADIENE is used as a monomer in the production of synthetic elastomers and resins, which are key components in the development of various types of polymers.
Used as a Solvent:
3-METHYL-1,4-PENTADIENE is used as a solvent in some industrial applications due to its ability to dissolve certain substances and facilitate chemical reactions.
Safety Precautions:
3-METHYL-1,4-PENTADIENE is considered a hazardous chemical and should be handled with caution due to its flammable and volatile nature. Proper safety measures, such as using protective equipment and following safety guidelines, should be taken to minimize risks during its use and handling.

Check Digit Verification of cas no

The CAS Registry Mumber 1115-08-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1115-08:
(6*1)+(5*1)+(4*1)+(3*5)+(2*0)+(1*8)=38
38 % 10 = 8
So 1115-08-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H10/c1-4-6(3)5-2/h4-6H,1-2H2,3H3

1115-08-8SDS

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 3-methylpenta-1,4-diene

1.2 Other means of identification

Product number -
Other names 3-methyl-penta-1,4-diene

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:1115-08-8 SDS

1115-08-8Related news

Ab initio study of C5H7 radicals involved in the photolyses of 3-methylcyclopentene and 3-METHYL-1,4-PENTADIENE (cas 1115-08-8) and 3-mythyl-1,4-pentadiene08/14/2019

The geometries of two trans- and two cis-2-vinylcycloprop-1-yl rotamers were optimized completely at the STO-3G level. The trans-(s-trans)2-vinylcycloprop-1-yl structure is predicted to be the most stable by both the STO-3G optimizations and by single-point 3-21G∗(5d)//STO-3G computations. The g...detailed

Asymmetric radiation-induced inclusion polymerization of 3-METHYL-1,4-PENTADIENE (cas 1115-08-8) in deoxycholic acid08/13/2019

The radiation-induced polymerization of 3-methyl-1,3-pentadiene (3MPD) as an inclusion complex in deoxycholic acid (DOCA) has produced in good yield the optically active polymer poly(3-methyl-1,4-pentadiene) (P3MPD) whose structure and properties were studied by FT-IR spectroscopy and thermal an...detailed

1115-08-8Relevant academic research and scientific papers

6- and 4-substituted-1-azabicyclo(3.2.0)heptan-3, 7-dione-2-carboxylates

-

, (2008/06/13)

Disclosed are 6- and 4-substituted-1-azabicyclo[3.2.0]heptan-3,7-dione-2-carboxylic acid esters and salts (I) which are useful in the preparation of 6-, 1- and 2-substituted carbapenem antibiotics. STR1 wherein R5 is a pharmaceutically acceptable ester moiety or a removable protecting group or an alkali or alkaline earth metal cation such as sodium or potassium and wherein R1, R2, Rhu 3 and R4 are, inter alia, independently selected from the group consisting of hydrogen, alkyl, aryl and aralkyl. Another embodiment disclosed is a group of compounds having the formula STR2 where X is a leaving group.

6-(1-hydroxyethyl)-2-(2-aminoethylthio)-1,1-disubstituted-1-carbadethiapen-2-em-3-carboxylic acids

-

, (2008/06/13)

Disclosed are 1-substituted-6-(1-hydroxyethyl)-2-(2-aminoethylthio)-1-carbadethiapen-2-em-3-carboxylic acids (I) and their pharmaceutically acceptable salts and esters which are useful as antibiotics; such compounds are prepared by total synthesis. STR1 wherein R1 and R2 are, inter alia, substituted and unsubstituted alkyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl and the spiro substituent formed by the joinder of R1 and R2.

Process for the preparation of carbapenem antibiotics

-

, (2008/06/13)

Disclosed is a process for the synthesis of carbapenem antibiotics I and their pharmaceutically acceptable salts and esters from 1: STR1 wherein: R7, R6, R1, R2 and R8 are selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, spirocycloalkyl, cycloalkylalkyl, alkylcycloalkyl, aryl, aralkyl, aralkenyl, aralkynyl, heteroalkyl, heteroaralkyl, heterocyclyl and heterocyclyalkyl.

6- And 1,1-disubstituted-1-carbadethiapen-2-em-3-carboxylic acid

-

, (2008/06/13)

Disclosed are 6- and 1-substituted-1-carbadethiapen-2-em-3-carboxylic acids I of the following structure: STR1 wherein R1, R2, R3 and R4 are, inter alia, independently selected from the group consisting of alkyl, aryl, and aralkyl. Such compounds as well as their pharmaceutically acceptable salt, ester and amide derivatives are useful as antibiotics. Also disclosed are processes for the preparation of such compounds, pharmaceutical compositions comprising such compounds and methods of treatment comprising administering such compounds and compositions when an antibiotic effect is indicated.

6-(1-Hydroxyethyl)-2-(2-aminoethylthio)-1,1-disubstituted-1-carbadethiapen-2-em-3-carboxylic acids

-

, (2008/06/13)

Disclosed are 1-substituted-6-(1-hydroxyethyl)-2-(2-aminoethylthio)-1-carbadethiapen-2-em-3-carboxylic acids (I) and their pharmaceutically acceptable salts and esters which are useful as antibiotics; such compounds are prepared by total synthesis. STR1 wherein R1 and R2 are, inter alia, substituted and unsubstituted alkyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl and the spiro substituent formed by the joinder of R1 and R2.

Mechanistic Aspects of Gas-Phase Photodecarbonylation Reactions of Bicyclohexanones

Mariano, Patrick S.,Bay, Elliott,Watson, Darrell G.,Rose, Timothy,Bracken, Christopher

, p. 1753 - 1762 (2007/10/02)

The gas-phase photodecarbonylation and photofragmentation reactions of substituted bicyclohexan-3-ones have been studied in detail.Photolysis of these ketones yields 1,3-dienes, vinylcyclopropanes, and 1,4-dienes as detectable products.The possible mechanisms for these reactions are discussed in light of the regiochemical and stereochemical results obtained.In addition, methyl substitution at C-6 and C-2 of these ketones has been shown to have a pronounced effect on both product ratios and overall reaction efficiency.These effects are discussed in terms of stereoelectronic and electronic controls of rates of cyclopropane ring opening of intermediate acylcyclopropylcarbinyl diradicals.

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