141968-99-2

Basic information

• Product Name: 1,3,2-Diazaphosphol-4-ene, 2-chloro-1,3-dibutyl-4,5-dimethyl-
• Synonyms: 1,3,2-Diazaphosphol-4-ene, 2-chloro-1,3-dibutyl-4,5-dimethyl-
• CAS NO: 141968-99-2
• Molecular Formula: C₁₂H₂₄ClN₂P
• Molecular Weight: 0
• Mol File: 141968-99-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 312°C at 760 mmHg
• Flash Point: 142.5°C
• Appearance: /
• Vapor Pressure: 0.000542mmHg at 25°C
• CAS DataBase Reference: 1,3,2-Diazaphosphol-4-ene, 2-chloro-1,3-dibutyl-4,5-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,2-Diazaphosphol-4-ene, 2-chloro-1,3-dibutyl-4,5-dimethyl-(141968-99-2)
• EPA Substance Registry System: 1,3,2-Diazaphosphol-4-ene, 2-chloro-1,3-dibutyl-4,5-dimethyl-(141968-99-2)

Safety Data

• Hazardous Substances Data: 141968-99-2(Hazardous Substances Data)

Usage

Chemical structure

Phosphorus-containing heterocyclic compound with a diazaphospholene ring

Functional groups

Chlorine atom, two butyl groups, and two methyl groups

Applications

a. Building block in organic synthesis
b. Ligand in coordination chemistry

Potential uses

a. Pharmaceuticals
b. Agrochemicals
c. Materials science

Current status

Specific functions and applications are still under investigation

InChI:InChI=1/C12H24ClN2P/c1-5-7-9-14-11(3)12(4)15(16(14)13)10-8-6-2/h5-10H2,1-4H3

Upstream product

• 589-57-1 diethyl phosphorylchloridite 
• 1498-42-6 phosphorodichloridous acid ethyl ester 
• 685-83-6 bis(diethylamino)chlorophosphine 
• 141968-97-0 1,3-Dibutyl-2-ethoxy-4,5-dimethyl-2,3-dihydro-1H-[1,3,2]diazaphosphole 

Downstream Products

• 109-69-3 n-Butyl chloride 
• 187090-99-9 1-Butyl-4,5-dimethyl-1H-[1,3,2]diazaphosphole 
• 141968-97-0 1,3-Dibutyl-2-ethoxy-4,5-dimethyl-2,3-dihydro-1H-[1,3,2]diazaphosphole 
• 141968-98-1 2-(diethylamino)-1,3-dibutyl-4,5-dimethyl-Δ⁴-1,3,2-diazaphospholine 

Relevant articles and documents

Chemical Properties of 1,3,2-Diazaphospholines

Δ4-1,3,2-Diazaphospholines exhibit properties typical of trivalent phosphorus derivatives: They take up sulfur, enter the Arbuzov, Perkow, and Staudinger reactions. On the other hand, these compounds show a number of peculiar features.