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1-(Butoxy-methoxy-phosphoryl)oxybutane is a complex organic compound with the molecular formula C10H23O5P. It is a phosphoric acid ester, specifically a derivative of phosphoric acid, where the hydroxyl group is replaced by a butoxy-methoxy-phosphoryl group. 1-(butoxy-methoxy-phosphoryl)oxybutane is characterized by its four oxygen atoms, one of which is part of a phosphorus-oxygen bond, and the other three are part of ether linkages. It is a colorless liquid with a low boiling point and is soluble in organic solvents. Due to its phosphorus content, it may have potential applications in the synthesis of pesticides, flame retardants, or as a chemical intermediate in various industrial processes. However, it is important to note that the compound's specific uses and properties would require further investigation and testing to ensure safety and efficacy.

7242-59-3

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7242-59-3 Usage

Chemical Class

Organophosphate

Use

Chemical weapon

Target

Human nervous system

Mechanism of Action

Inhibits the enzyme acetylcholinesterase

Effect on Nervous System

Causes an accumulation of the neurotransmitter acetylcholine and overstimulation

Symptoms of Exposure

Respiratory distress, convulsions, and death

Banned Substance

Yes, under the Chemical Weapons Convention

Classification

Schedule 1 substance by the Chemical Weapons Convention

Check Digit Verification of cas no

The CAS Registry Mumber 7242-59-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,4 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7242-59:
(6*7)+(5*2)+(4*4)+(3*2)+(2*5)+(1*9)=93
93 % 10 = 3
So 7242-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H28O3/c1-11-13-9-12-5-6-16-19(2,3)17(21)7-8-20(16,4)14(12)10-15(13)23-18(11)22/h9,14-17,21H,5-8,10H2,1-4H3

7242-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dibutyl methyl phosphate

1.2 Other means of identification

Product number -
Other names Phosphoric acid,dibutyl methyl ester

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:7242-59-3 SDS

7242-59-3Relevant academic research and scientific papers

Phosphadioxirane Intermediates in the Reaction of Singlet Oxygen with Phosphites and Phosphines

Tsuji, Shoei,Kondo, Masaaki,Ishiguro, Katsuya,Sawaki, Yasuhiko

, p. 5055 - 5059 (2007/10/02)

Intermediates in the singlet oxygen reaction of phosphites and phosphines have been studied by trapping and tracer experiments.Trapping study with diphenyl sulfoxide revealed that the added substrate and phosphite are competing toward the same intermediate.The relative reactivity of (BuO)3P/Ph2S/Ph2SO = 300:4:1 and the negative ρ-value of -0.63 for diphenyl sulfoxides are not consistent with 1,3-dipolar phosphine peroxides, but suggest electrophilic O-transfers by cyclic phosphadioxiranes.Intermediacy of phosphadioxiranes was supported by an 18O-tracer study on the formation of rearranged diphenylphosphinate from 1O2 and triphenylphosphine.Theoretical calculations also supported the dioxirane intermediate by predicting no existence of 1,3-dipolar peroxide.

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