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Phosphine oxide, bis(m-aminophenyl)methyl-, also known as 1,1-bis(3-aminophenyl)methylphosphine oxide, is an organic compound with the chemical formula C19H18NOP. It is a colorless to pale yellow crystalline solid that is soluble in common organic solvents such as ethanol, acetone, and dichloromethane. Phosphine oxide, bis(m-aminophenyl)methyl- is primarily used as a ligand in coordination chemistry, particularly in the formation of transition metal complexes. It is known for its ability to stabilize metal centers and can be used in the synthesis of various catalysts and materials with potential applications in fields such as catalysis, materials science, and pharmaceuticals. The compound is also of interest due to its potential use in the development of new drugs and its role in organophosphorus chemistry.

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  • 783-81-3 Structure
  • Basic information

    1. Product Name: Phosphine oxide, bis(m-aminophenyl)methyl-
    2. Synonyms:
    3. CAS NO:783-81-3
    4. Molecular Formula:
    5. Molecular Weight: 246.249
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 783-81-3.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: Phosphine oxide, bis(m-aminophenyl)methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phosphine oxide, bis(m-aminophenyl)methyl-(783-81-3)
    11. EPA Substance Registry System: Phosphine oxide, bis(m-aminophenyl)methyl-(783-81-3)
  • 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: 783-81-3(Hazardous Substances Data)

783-81-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 783-81-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 783-81:
(5*7)+(4*8)+(3*3)+(2*8)+(1*1)=93
93 % 10 = 3
So 783-81-3 is a valid CAS Registry Number.

783-81-3SDS

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 Bis(m-aminophenyl)methylphosphine oxide

1.2 Other means of identification

Product number -
Other names -

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:783-81-3 SDS

783-81-3Downstream Products

783-81-3Relevant articles and documents

Voltage Imaging with a NIR-Absorbing Phosphine Oxide Rhodamine Voltage Reporter

Gonzalez, Monica A.,Walker, Alison S.,Cao, Kevin J.,Lazzari-Dean, Julia R.,Settineri, Nicholas S.,Kong, Eui Ju,Kramer, Richard H.,Miller, Evan W.

, p. 2304 - 2314 (2021/02/16)

The development of fluorescent dyes that emit and absorb light at wavelengths greater than 700 nm and that respond to biochemical and biophysical events in living systems remains an outstanding challenge for noninvasive optical imaging. Here, we report the design, synthesis, and application of near-infrared (NIR)-absorbing and -emitting optical voltmeter based on a sulfonated, phosphine-oxide (po) rhodamine for voltage imaging in intact retinas. We find that po-rhodamine based voltage reporters, or poRhoVRs, display NIR excitation and emission profiles at greater than 700 nm, show a range of voltage sensitivities (13 to 43% ΔF/F per 100 mV in HEK cells), and can be combined with existing optical sensors, like Ca2+-sensitive fluorescent proteins (GCaMP), and actuators, like light-activated opsins ChannelRhodopsin-2 (ChR2). Simultaneous voltage and Ca2+ imaging reveals differences in activity dynamics in rat hippocampal neurons, and pairing poRhoVR with blue-light based ChR2 affords all-optical electrophysiology. In ex vivo retinas isolated from a mouse model of retinal degeneration, poRhoVR, together with GCaMP-based Ca2+ imaging and traditional multielectrode array (MEA) recording, can provide a comprehensive physiological activity profile of neuronal activity, revealing differences in voltage and Ca2+ dynamics within hyperactive networks of the mouse retina. Taken together, these experiments establish that poRhoVR will open new horizons in optical interrogation of cellular and neuronal physiology in intact systems.

Systematic study of synthesizing various heteroatom-substituted rhodamines from diaryl ether analogues

Deng, Fei,Huang, Chunfang,Huang, Wei,Liu, Limin,Qiao, Qinglong,Xu, Zhaochao

, (2020/06/09)

The dye rhodamine, as the most popular scaffold to construct fluorescent labels and probes, has been explored extensively on its structure-fluorescence relationships. Particularly, the replacement of the oxygen atom in the 10th position with heteroatoms obtained various new rhodamines with improved photophysical properties, such as brightness, photostability, red-shifted emission and fluorogenicity. However, the applications of heteroatom-substituted rhodamines have been hindered by difficult synthetic routes. Herein, we explored the condensation strategy of diaryl ether analogues and o-tolualdehyde to synthesize various heteroatom-substituted rhodamines. We found that the electron property and steric effect in the rhodamine 10th position determined the synthetic yield. It's concluded that this condensation method was more suitable for the synthesis of heteroatom-substituted rhodamines with small or electron-donating groups like rhodamine, S-rhodamine and Si-rhodamine. We hope these results will benefit the design and synthesis of heteroatom-substituted rhodamines.

Development of improved dual-diazonium reagents for faster crosslinking of tobacco mosaic virus to form hydrogels

Ma, Dejun,Chen, Zhuoyue,Yi, Long,Xi, Zhen

, p. 29070 - 29077 (2019/09/30)

New bench-stable reagents with two diazonium sites were designed and synthesized for protein crosslinking. Because of the faster diazonium-tyrosine coupling reaction, hydrogels from the crosslinking of tobacco mosaic virus and the reagent DDA-3 could be p

Synthesis and properties of novel polyimide fibers containing phosphorus groups in the main chain

Zhao, Yong,Feng, Tao,Li, Guomin,Liu, Fangfang,Dai, Xuemin,Dong, Zhixin,Qiu, Xuepeng

, p. 42482 - 42494 (2016/05/19)

A series of polyamic acid copolymers (co-PAAs) containing phosphorous groups in the main chain were synthesized using different ratios of two diamines, i.e., bis(3-aminophenyl)methyl phosphine oxide (DAMPO) and 4,4′-oxydianiline (ODA), with 3,3′,4,4′-biphenyltetracarboxylic dianhydride (s-BPDA) by polycondensation in N,N′-dimethyacetamide (DMAc). The co-PAA solutions were spun into fibers by a dry-jet wet spinning process, and then polyimide copolymer (co-PI) fibers were obtained by thermal imidization. ATR-FTIR spectra and elemental analysis confirmed the chemical structure of PAA and PI fibers. The as-prepared PI fibers have smooth and dense surface as well as uniform diameter. Compared with the blank PI-0, the Tg values of co-PI fibers increased considerably with the increase in DAMPO content. TGA results indicated that the co-PI fibers possessed good thermal stability up to 510 °C and a residual char yield of up to 61% at 850 °C. All co-PI fibers exhibited excellent elongation, and their tensile strength and modulus can reach 0.9 GPa and 14.97 GPa when the molar ratio of DAMPO/ODA was 6/4 and the draw ratio was 3.0. The relationship between microstructure and mechanical property is also discussed.

Near-Infrared Phosphorus-Substituted Rhodamine with Emission Wavelength above 700 nm for Bioimaging

Chai, Xiaoyun,Cui, Xiaoyan,Wang, Baogang,Yang, Fan,Cai, Yi,Wu, Qiuye,Wang, Ting

supporting information, p. 16754 - 16758 (2015/11/16)

Phosphorus has been successfully fused into a classic rhodamine framework, in which it replaces the bridging oxygen atom to give a series of phosphorus-substituted rhodamines (PRs). Because of the electron-accepting properties of the phosphorus moiety, wh

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