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13151-04-7

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13151-04-7 Usage

Description

5-Methyl-1-heptene, also known as 1-heptene-5-methyl or 5-methylhept-1-ene, is a branched-chain alkene with the molecular formula C8H16. It is classified as an alpha-olefin and is characterized by its colorless liquid form, mild odor, and flammable nature. This chemical is relatively stable under normal conditions but requires careful handling and storage away from ignition sources and incompatible materials. 5-Methyl-1-heptene is a versatile chemical with a range of industrial applications, including the production of synthetic rubber and plastics, as well as serving as a solvent and a chemical intermediate in the synthesis of various organic compounds.

Uses

Used in Chemical Synthesis Industry:
5-Methyl-1-heptene is used as a chemical intermediate for the synthesis of various organic compounds, contributing to the development of new materials and products.
Used in Plastics and Rubber Industry:
5-Methyl-1-heptene is used as a key component in the production of synthetic rubber and plastics, enhancing the versatility and performance of these materials.
Used as a Solvent:
5-Methyl-1-heptene is utilized as a solvent in various industrial processes, facilitating chemical reactions and material processing.
Used in Research and Development:
5-Methyl-1-heptene serves as a valuable compound in research and development, enabling scientists to explore its properties and potential applications in different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 13151-04-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,5 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13151-04:
(7*1)+(6*3)+(5*1)+(4*5)+(3*1)+(2*0)+(1*4)=57
57 % 10 = 7
So 13151-04-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H16/c1-4-6-7-8(3)5-2/h4,8H,1,5-7H2,2-3H3

13151-04-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methylhept-1-ene

1.2 Other means of identification

Product number -
Other names 2-Ethyl-1-hexen

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:13151-04-7 SDS

13151-04-7Relevant articles and documents

Synthesis and transformations of metallacycles 46. Catalytic cycloalumination reaction in the synthesis of bis(phospholanes)

D’yakonov,Makhamatkhanova,Agliullina,Tyumkina,Dzhemilev

, p. 2493 - 2497 (2016/09/28)

An efficient one-pot synthesis of bis(phospholanes) was elaborated, which included a sequential Cp2ZrCl2-catalyzed cycloalumination of α,ω-diolefins with AlEt3, giving the corresponding bis(aluminacyclopentanes), and their in situ reaction with dihalophosphines to furnish the target α,ω-bis(phospholanes). The reaction of these compounds with H2O2 or elementary sulfur gave the corresponding bis(phospholane 1-oxides) and bis(phospholane 1-sulfides).

Cyclization of methyl-substituted 6-heptenyl radicals

Bailey, William F.,Longstaff, Sarah C.

, p. 2217 - 2219 (2007/10/03)

(Matrix presented) The behavior of a series of methyl-substituted 6-heptenyl radicals, generated from the corresponding iodides ((Me3Si)3SiH, AIBN in benzene at 80°C), has been investigated. The stereoselectivity of the 6-exo cyclizations, affording dimethylcyclohexanes, is low, and sizable quantities of methylcycloheptane, generated via 7-endo cyclization, are also produced.

SYNTHETIC INVESTIGATIONS INTO INSECT-ATTRACTING SUBSTANCES (SEX ATTRACTANTS). IV. SYNTHESIS OF 14-METHYL-8-cis-HEXADECENAL AND 14-METHYL-8-trans-HEXADECENAL, COMPONENTS OF THE SEX PHEROMONE OF THE DERMESTID BEETLE Trogoderma granarium EVERTS

Kovalev, B. G.,Rastegaeva, V. M.

, p. 44 - 47 (2007/10/02)

14-Methyl-8-hexadecyn-1-ol was obtained by the alkylation of 7-methyl-1-nonyne with heptamethylene chlorohydrin.Its hydrogenation in the presence of colloidal nickel catalyst was used for the synthesis of 14-methyl-8-cis-hexadecen-1-ol, and reduction with lithium aluminum hydride was used for the synthesis of 14-methyl-8-trans-hexadecen-1-ol.Both ethylenic alcohols were converted by oxidation into the corresponding aldehydes, which are the main components of the sex pheromone of the dermestid beetle.

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