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1-(diethylamino)-3-(prop-2-en-1-yloxy)propan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14112-80-2

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14112-80-2 Usage

Type of compound

synthetic chemical compound

Usage

reagent in organic chemical synthesis

Functional groups

a. Alcohol derivative
b. Diethylamino group
c. Prop-2-en-1-yloxy group

Carbon chain

attached functional groups

Potential applications

a. Pharmaceutical industry (new drugs)
b. Agricultural industry (pesticides)

Safety precautions

handle with care, hazardous if not used properly

Check Digit Verification of cas no

The CAS Registry Mumber 14112-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,1 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14112-80:
(7*1)+(6*4)+(5*1)+(4*1)+(3*2)+(2*8)+(1*0)=62
62 % 10 = 2
So 14112-80-2 is a valid CAS Registry Number.

14112-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(diethylamino)-3-prop-2-enoxypropan-2-ol

1.2 Other means of identification

Product number -
Other names 1-(diethylamino)-3-(prop-2-en-1-yloxy)propan-2-ol

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:14112-80-2 SDS

14112-80-2Downstream Products

14112-80-2Relevant academic research and scientific papers

Aluminium triflate: an efficient recyclable Lewis acid catalyst for the aminolysis of epoxides

Williams, D. Bradley G.,Lawton, Michelle

, p. 6557 - 6560 (2007/10/03)

Epoxides are powerful starting materials for a range of useful materials and can be converted into, amongst others, amino alcohols. In this work, a range of epoxides was ring-opened using various alkyl- and arylamines under the action of aluminium triflat

A new and efficient epoxide ring opening via poor nucleophiles: Indole, p-nitroaniline, borane and O-trimethylsilylhydroxylamine in lithium perchlorate

Heydari, Akbar,Mehrdad, Morteza,Maleki, Aziz,Ahmadi, Nafiseh

, p. 1563 - 1565 (2007/10/03)

Highly regioselective ring opening of 2,3-dimethyloxirane, 2-epoxyphenylether and allyl(2-epoxymethyl) ether are observed through reactions with poor nucleophiles such as indole, borane, O-trimethylsilylhydroxylamine, p-nitroaniline and sterically hindered tert-butylamine in the presence of 5.0 M lithium perchlorate-Et2O solution. These reactions are fast, convenient, with rather high yields and are carried out at ambient temperatures.

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