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6937-25-3

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6937-25-3 Usage

Chemical Properties

Nsc41608 is Colorless Oil

Uses

Different sources of media describe the Uses of 6937-25-3 differently. You can refer to the following data:
1. 2,2''-Oxybis-propanoic Acid Diethyl Ester is an intermediate used in the preparation of the organochlorine pesticide Bis(2-chloroisopropyl) Ether (B419020(M)). Bis(2-chloroisopropyl) Ether is used as a nematicide to control parasitic nematodes in agriculture.
2. Nsc41608 is an intermediate used in the preparation of the organochlorine pesticide Bis(2-chloroisopropyl) Ether.

Check Digit Verification of cas no

The CAS Registry Mumber 6937-25-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6937-25:
(6*6)+(5*9)+(4*3)+(3*7)+(2*2)+(1*5)=123
123 % 10 = 3
So 6937-25-3 is a valid CAS Registry Number.

6937-25-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(1-ethoxy-1-oxopropan-2-yl)oxypropanoate

1.2 Other means of identification

Product number -
Other names diethyl 2,2-dioctylmalonate

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:6937-25-3 SDS

6937-25-3Relevant articles and documents

Cyclopropanespiro-β-lactones derived from 4-[(Z)-ethylidene]-3- methyloxetan-2-one: Diastereoselective formation and rearrangement reactions

Geraghty, Niall W.A.,McArdle, Patrick,Mullen, Laverne M.A.

experimental part, p. 3546 - 3552 (2011/06/11)

The metal catalysed reaction of monosubstituted diazo esters and ketones with 4-[(Z)-ethylidene]-3-methyloxetan-2-one results in the formation of cyclopropanespiro-β-lactones. In contrast to most alkene cyclopropanations, including those involving diketene, the reaction occurs diastereoselectively. A computational model of the reaction has been developed that accounts for the observed stereochemistry. The metal promoted thermal rearrangement of these spiro compounds is also unusual in that it affords pyranones, rather than the decarboxylation products characteristic of β-lactones in general, or the furanones formed from diketene derived cyclopropanespiro-β-lactones.

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