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1-(1-ethoxyethoxy)pentane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13442-89-2

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13442-89-2 Usage

Definition

ChEBI: A dieter that is 1-pentoxyethane substituted by an ethoxy group at position 1.

Check Digit Verification of cas no

The CAS Registry Mumber 13442-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,4 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13442-89:
(7*1)+(6*3)+(5*4)+(4*4)+(3*2)+(2*8)+(1*9)=92
92 % 10 = 2
So 13442-89-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O2/c1-4-6-7-8-11-9(3)10-5-2/h9H,4-8H2,1-3H3

13442-89-2SDS

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 1-ethoxy-1-pentoxyethane

1.2 Other means of identification

Product number -
Other names Pentane, 1-(1-ethoxyethoxy)-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:13442-89-2 SDS

13442-89-2Downstream Products

13442-89-2Relevant academic research and scientific papers

Electrophilic Addition to Alkoxyethenes. XV. Influence of Structure and Temperature on the Rate of Ethanol Addition

Nedolya, N. A.,Baranskii, V. A.,Trofimov, B. A.

, p. 287 - 290 (2007/10/03)

Rates of acid-catalyzed (in the presence of HCl) addition of ethanol to various alkyl vinyl ethers in the system cyclohexane-ethanol (4:1 by volume) have been measured at 10, 20, 25, 30, and 40 deg C.Linear regression equations have been found that adequately describe the influence of temperature and the substrate structure on the rate constant.The effect of the alkyl substituents includes variable contribution of the steric factor; bulky substituents facilitate the reaction.

WITTIG-HORNER REACTION IN HETEROGENOUS MEDIA VII. A NEW STRATEGY FOR THE TOTAL SYNTHESIS OF THE ROYAL JELLY ACID AND THE QUEEN SUBSTANCE OF HONEY-BEE

Villieras, J.,Rambaud, M.,Graff, M.

, p. 569 - 580 (2007/10/02)

A new general scheme for the preparation of Royal Jelly acid and Queen Substance of honey-bee, including, as the key steps, copper I catalyzed addition of functional (protected alcohol and ketone) Grignard reagents to acrolein diethylacetal, and the Wittig-Horner reaction of unprotected 8-hydroxyoctanal and 7-oxo-octanal with triethylphosphonoacetate in water, in the presence of potassium carbonate.

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