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2-chloroethoxyacetonitrile, also known as 2-(2-chloroethoxy)acetonitrile, is an organic compound that serves as a key intermediate in the synthesis of various pharmaceuticals. It is characterized by its reactivity and functional groups, which make it a versatile building block in the development of new drugs.

31250-08-5

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31250-08-5 Usage

Uses

Used in Pharmaceutical Industry:
2-chloroethoxyacetonitrile is used as a synthetic intermediate for the preparation of levocetirizine and its intermediates. Levocetirizine is a second-generation antihistamine used to treat symptoms of allergies such as sneezing, runny nose, and itchy eyes. 2-chloroethoxyacetonitrile's reactivity and functional groups make it an essential component in the synthesis of this medication, contributing to its effectiveness in alleviating allergic symptoms.

Check Digit Verification of cas no

The CAS Registry Mumber 31250-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,5 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 31250-08:
(7*3)+(6*1)+(5*2)+(4*5)+(3*0)+(2*0)+(1*8)=65
65 % 10 = 5
So 31250-08-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H6ClNO/c5-1-3-7-4-2-6/h1,3-4H2

31250-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-chloroethoxy)acetonitrile

1.2 Other means of identification

Product number -
Other names 2-chloroethyl cyanomethyl 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:31250-08-5 SDS

31250-08-5Relevant academic research and scientific papers

A high-purity 4 - (4 - aminophenyl) morpholine -3 - ketone (by machine translation)

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Paragraph 0069; 0070, (2019/03/15)

The invention relates to a low-cost, high-purity of 4 - (4 - aminophenyl) morpholine - 3 - one (II) of the preparation method. The use of hydroxy acetonitrile and 1, 2 - dihalo substituted ethane in the reaction process for preparing halogenated ethyl oxygen radical second grade nitrile IV, then with the para-nitroaniline III substituted reaction, acid lower ring becomes a 4 - (4 - nitrophenyl) morpholine - 3 - ketone V, 4 - (4 - nitrophenyl) morpholine - 3 - ketone V obtained by hydrogenating and reducing 4 - (4 - aminophenyl) morpholine - 3 - one II. The present invention the used raw materials are cheap and easily obtained, and the cost is low; the process route is simple, safety and environmental protection; the design of each step the reaction selectivity is high, high yield, high purity for the 4 - (4 - aminophenyl) morpholine - 3 - ketone preparation provides a guarantee, to industrial production of high-purity [...]. (by machine translation)

Complexes of macrocyclic compounds

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, (2008/06/13)

Novel macrocyclic (monocyclic and bicyclic) compounds having nitrogen bridgehead atoms and having in the hydrocarbon bridging chains at least two additional hetero atoms selected from the group consisting of sulfur, oxygen, and nitrogen, when admixed with a compatible cation-donor compound form stable cation-containing macrocyclic complexes which, in turn, can be conveniently dissociated by addition of acid or a quaternizing agent. The novel macrocyclics are valuable for use in the same way and for the same purposes as chelating agents.

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