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Vinyl decyl ether, also known as decyl vinyl ether or 1-decen-1-yl ethyl ether, is a colorless liquid with the chemical formula C12H24O. It is an ether derivative formed by the reaction of decanol and vinyl ethyl ether. This organic compound is characterized by a vinyl group (C2H3) attached to a decyl chain (C10H21), which gives it unique properties. It is used in the synthesis of various chemicals, particularly in the production of surfactants, lubricants, and plasticizers. Due to its reactive vinyl group, vinyl decyl ether can also be polymerized, making it a potential monomer for the creation of polymers with specific properties. It is important to handle this chemical with care, as it can be harmful if inhaled or absorbed through the skin, and it is flammable.

58335-26-5

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58335-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58335-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,3 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58335-26:
(7*5)+(6*8)+(5*3)+(4*3)+(3*5)+(2*2)+(1*6)=135
135 % 10 = 5
So 58335-26-5 is a valid CAS Registry Number.

58335-26-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Vinyloxy)decane

1.2 Other means of identification

Product number -
Other names 1-decenyl ethyl ether

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:58335-26-5 SDS

58335-26-5Upstream product

58335-26-5Downstream Products

58335-26-5Relevant academic research and scientific papers

Solvolysis of 1-decenyl(phenyl)iodonium tetrafluoroborate: Mechanisms of nucleophilic substitution and elimination

Okuyama, Tadashi,Imamura, Shohei,Ishida, Yoshimi

, p. 543 - 548 (2001)

Solvolysis of (E)-1-decenyl(phenyl)iodonium tetrafluoroborate 1 was carried out in some alcohols, acetic acid, and mixed aqueous alcoholic solvents at 50-60°C and the effects of added carboxylates and other salts were also examined in methanol. Reaction products include enol derivatives (substitution) and 1-decyne (elimination) as well as iodobenzene. Rates for the solvolysis increase with increasing nucleophilicity of the solvent but have no correlation with the solvent ionizing power. The substitution occurs mostly via inversion of configuration, and is concluded to follow the in-plane SN2 mechanism with a minor concomitant out-of-plane SN2 pathway. The reactions with the deuterated substrates show that stronger bases of pKa of the conjugate acid > 3 induce exclusively α-elimination of 1 in methanol. However, both α- and β-elimination occur in neutral methanol in a ratio of about 3/1 besides the substitution. Mechanisms for these reactions are proposed.

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