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85721-25-1

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85721-25-1 Usage

Description

1,2-Epoxy-9-decene is an unsaturated epoxide characterized by the presence of a carbon-carbon double bond and an epoxy group. It is a clear, colorless liquid with unique chemical properties that make it suitable for various applications.

Uses

Used in Chemical Synthesis:
1,2-Epoxy-9-decene is used as a key intermediate in the synthesis of various organic compounds. Its unsaturated nature allows for hydrogenation reactions, such as the hydrogenation of the C=C bond over palladium nanoparticles (PdOAc,N), to produce valuable chemical products.
Used in Polymer Industry:
1,2-Epoxy-9-decene is used as a monomer in the production of polymers. Its epoxy group can undergo polymerization reactions, leading to the formation of polymers with specific properties, such as adhesion, flexibility, and thermal stability.
Used in Pharmaceutical Industry:
1,2-Epoxy-9-decene is used as a building block in the synthesis of pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Flavor and Fragrance Industry:
1,2-Epoxy-9-decene is used as a precursor in the production of natural flavors and fragrances. Its ability to undergo various chemical reactions enables the creation of complex and diverse scent profiles.
Used in Adhesive and Sealant Industry:
1,2-Epoxy-9-decene is used as a component in the formulation of adhesives and sealants. Its reactive epoxy group allows for the formation of strong bonds with various substrates, providing excellent adhesion and sealing properties.

Check Digit Verification of cas no

The CAS Registry Mumber 85721-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,7,2 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85721-25:
(7*8)+(6*5)+(5*7)+(4*2)+(3*1)+(2*2)+(1*5)=141
141 % 10 = 1
So 85721-25-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-2-3-4-5-6-7-8-10-9-11-10/h2,10H,1,3-9H2/t10-/m0/s1

85721-25-1 Well-known Company Product Price

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  • Aldrich

  • (410829)  1,2-Epoxy-9-decene  96%

  • 85721-25-1

  • 410829-25ML

  • 1,261.26CNY

  • Detail

85721-25-1SDS

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 1,2-EPOXY-9-DECENE

1.2 Other means of identification

Product number -
Other names 2-oct-7-enyloxirane

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:85721-25-1 SDS

85721-25-1Relevant articles and documents

Synthesis and characterization of a new poly α-amino acid Co(II)-complex supported on magnetite graphene oxide as an efficient heterogeneous magnetically recyclable catalyst for efficient free-coreductant gram-scale epoxidation of olefins with molecular oxygen

Kazemnejadi, Milad,Mahmoudi, Boshra,Sharafi, Zeinab,Nasseri, Mohammad Ali,Allahresani, Ali,Esmaeilpour, Mohsen

, p. 59 - 69 (2019/06/13)

A novel magnetic nanocomposite was prepared by immobilization of a cobalt complex of a synthetic poly α-amino acid on Fe3O4-doped graphene oxide (GO/Fe3O4@PAA Co(II)) and was demonstrated to be a highly efficient catalyst for the epoxidation of olefins in mild conditions. PAA was synthesized through a multi-step synthesis, first by a poly condensation reaction of salicylaldehyde followed by the Strecker synthesis. The synthesized nanocomposite was characterized by various analytical and spectroscopic methods including FTIR, ICP, XRD, EDX, XPS, FE-SEM, TEM, TGA, VSM and DLS analyses. A wide variety of olefins could be tolerated toward epoxidation in the presence of molecular oxygen without the need for any co-reductant. The magnetic nanocomposite could be readily separated by a magnet from the mixture and reused for several times without any significant reactivity loss, which represents its potential for practical and industrial application. Also, the scalability of the process was investigated in this work.

An efficient epoxidation of terminal aliphatic alkenes over heterogeneous catalysts: When solvent matters

Palumbo,Tiozzo,Ravasio,Psaro,Carniato,Bisio,Guidotti

, p. 3832 - 3839 (2016/06/13)

The epoxidation of unfunctionalized terminal aliphatic alkenes over heterogeneous catalysts is still a challenging task. Due to the tuning of a peculiar catalyst/oxidant/solvent combination, it was possible to attain good alkene conversions (73%) and excellent selectivity values (>98%) in the desired terminal 1,2-epoxide. Over the titanium-silica catalyst and in the presence of tert-butylhydroperoxide, the use of α,α,α-trifluorotoluene as an uncommon non-toxic solvent was the key factor for a marked enhancement of selectivity. The titanium-silica catalyst was efficiently recycled and reused after a gentle rinsing with fresh solvent.

Electroorganic synthesis 65. Anodic homocoupling of carboxylic acids derived from fatty acids

Weiper-Idelmann, Andreas,Aus Dem Kahmen, Martin,Schaefer, Hans J.,Gockeln, Marianne

, p. 672 - 682 (2007/10/03)

Fatty acid derived carboxylic acids with double bonds, hydroxy-, amino-, keto-, ester- and epoxy groups are anodically coupled to dimers (Kolbe electrolysis) in 29 to 81% yield and up to a 2.5 mol scale. Problems due to the low conductivity of fatty acid salts were overcome by the use of a flow cell with a narrow electrode gap. Fatty acids with branched alkyl chains gave dimers with interesting emulsifying properties. Dimethyl hexadecanedioate, accessible from methyl azelate, could be cyclized and further converted into homomuscone and muscone in a few steps. A commercial mixture of dimeric fatty acids (C36-dicarboxylic acids) has been coupled to give C70-diesters. Acta Chemica Scandinavica 1998. Part 64: Nielsen, M. F., Batanero, B.,.

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