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2-methoxy-4-methyl-1,3,2-dioxaphospholane 2-oxide is an organophosphorus compound with the molecular formula C4H9O4P and a molecular weight of 152.07 g/mol. It is a colorless liquid with a boiling point of 90-92°C and a flash point of 31°C.

26964-04-5

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26964-04-5 Usage

Uses

Used in Pharmaceutical Industry:
2-methoxy-4-methyl-1,3,2-dioxaphospholane 2-oxide is used as an intermediate in the synthesis of various drugs. Its unique chemical structure allows it to be a versatile building block for the development of new pharmaceutical compounds.
Used in Agricultural Industry:
2-methoxy-4-methyl-1,3,2-dioxaphospholane 2-oxide is used in the production of pesticides. Its reactivity and stability make it a valuable component in the formulation of effective and safe agricultural chemicals.
It is important to handle 2-methoxy-4-methyl-1,3,2-dioxaphospholane 2-oxide with care, as it can be hazardous if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 26964-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,6 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26964-04:
(7*2)+(6*6)+(5*9)+(4*6)+(3*4)+(2*0)+(1*4)=135
135 % 10 = 5
So 26964-04-5 is a valid CAS Registry Number.

26964-04-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxy-4-methyl-1,3,2λ<sup>5</sup>-dioxaphospholane 2-oxide

1.2 Other means of identification

Product number -
Other names 2-methoxy-4-methyl-1,3,2

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:26964-04-5 SDS

26964-04-5Downstream Products

26964-04-5Relevant academic research and scientific papers

Reaction of Epoxides with Metaphosphoric Acid Derivatives

Bodalski, Ryszard,Quin, Louis D.

, p. 2666 - 2671 (2007/10/02)

Ethyl metaphosphate (EtOPO2), eliminated in the thermolysis of the bridged cyclic phosphonate endo-3-ethoxy-6-methyl-N-phenyl-2,3-oxabicyclooct-5-ene-8,9-dicarboximide 3-oxide, has been found to cause ring opening of epoxides, resulting in formation of 2-ethoxy-4-substituted 1,3,2-dioxaphospholane 2-oxides as major products.N,N-Diethyl metaphosphoramidate (Et2NPO2) reacted similarly.With ethyl metathiophosphate (EtOP(S)O), the 1,3,2-oxathiaphospholane 2-oxide ring was formed.Products of these reactions were characterized by 31P NMR spectroscopy and by GC-MS.These reactions are presumed to be initiated by electrophilic attack of the metaphosphate on the epoxide oxygen to form a cyclic oxonium ion.

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