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CAS

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3576-20-3

2,2,2-Trichloro-1,3-dimethyl-1,3,2λ5-diazaphosphetidin-4-one is a cyclic phosphorylated compound derived from the reaction of phosphorus pentachloride (PCl5) with N,N'-dialkylureas, specifically N-methyl-N'-chloroacetylurea, where the N-acetyl fragment undergoes chlorination during the process. This heterocyclic structure features a phosphorus center bonded to three chlorine atoms and incorporated into a diazaphosphetidinone ring system with two methyl substituents on the nitrogen atoms. 2,2,2-trichloro-1,3-dimethyl-1,3,2lambda~5~-diazaphosphetidin-4-one is representative of a class of trichlorodiazaphosphetidinones formed through the phosphorylation of ureas.

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  • 3576-20-3 Structure

  • Basic information

    1. Product Name: 2,2,2-trichloro-1,3-dimethyl-1,3,2lambda~5~-diazaphosphetidin-4-one
    2. Synonyms: 1,3,2-Diazaphosphetidin-4-one, 2,2,2-trichloro-2,2-dihydro-1,3-dimethyl-
    3. CAS NO:3576-20-3
    4. Molecular Formula: C3H6Cl3N2OP
    5. Molecular Weight: 223.4253
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3576-20-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,2,2-trichloro-1,3-dimethyl-1,3,2lambda~5~-diazaphosphetidin-4-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2,2-trichloro-1,3-dimethyl-1,3,2lambda~5~-diazaphosphetidin-4-one(3576-20-3)
    11. EPA Substance Registry System: 2,2,2-trichloro-1,3-dimethyl-1,3,2lambda~5~-diazaphosphetidin-4-one(3576-20-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 3576-20-3(Hazardous Substances Data)

3576-20-3 Usage

Type of compound

Organophosphate insecticide and acaricide

Uses

Control of pests in agriculture, including flies, fleas, and ticks on livestock, and as a larvicide for controlling mosquitoes in water

Toxicity

Moderately toxic to humans

Mechanism of action

Inhibitor of cholinesterase, an enzyme essential for proper nerve function

Symptoms of exposure

Headache, dizziness, nausea, and muscle weakness

Safety precautions

Should be used according to proper safety guidelines and regulations.

Check Digit Verification of cas no

The CAS Registry Mumber 3576-20-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,7 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3576-20:
(6*3)+(5*5)+(4*7)+(3*6)+(2*2)+(1*0)=93
93 % 10 = 3
So 3576-20-3 is a valid CAS Registry Number.

3576-20-3SDS

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 2,2,2-trichloro-1,3-dimethyl-1,3,2λ<sup>5</sup>-diazaphosphetidin-4-one

1.2 Other means of identification

Product number -
Other names 2,2,2-trichloro-1,3-dimethyldiazaphosphetidinone

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:3576-20-3 SDS

3576-20-3Upstream product

3576-20-3Relevant articles and documents

REACTIONS OF PHOSPHORUS PENTACHLORIDE WITH N,N'-DIALKYL- AND N-ALKYL-N'-ACETYLUREAS

Timokhin, B. V.,Dmitriev, V. K.,Dmitrichenko, M. Yu.,Dolgushin, G. V.

, p. 170 - 172 (1991)

N,N'-dialkylureas are phosphorylated by phosphorus pentachloride to give cyclic trichlorodiazaphosphetidinones.The formation of these derivatives in the reaction of N-methyl-N'-chloroacetylurea with PCl5 is accompanied by the chlorination of the N-acetyl fragment.

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