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1,3-dimethyl-N,N-di(propan-2-yl)-1,3-dihydro-2H-1,3,2-benzodiazaphosphol-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79607-90-2

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79607-90-2 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 14 carbon (C), 26 hydrogen (H), 2 nitrogen (N), and 1 phosphorus (P) atoms.

Explanation

This is the IUPAC name of the compound, which describes the arrangement of atoms and functional groups in the molecule.

Explanation

The compound contains a phosphorus atom bonded to two nitrogen and three carbon atoms, classifying it as a phosphazene compound.

Explanation

The compound's properties make it suitable for various industrial uses, such as improving the fire resistance of materials, enhancing the performance of lubricants, and serving as a starting material for the production of other phosphorus-based compounds.

Explanation

The compound features a benzodiazaphosphol ring, which is a fused ring system consisting of a benzene ring and a diazaphosphole ring.

Explanation

Due to its unique structure and properties, the compound can be applied in multiple industries, making it a versatile chemical.

Explanation

The compound has several functional groups, including two methyl groups (-CH3), two propyl groups (-C3H7), and an amine group (-NH2), which contribute to its chemical properties and reactivity.

Explanation

Based on the molecular formula and the presence of multiple carbon and hydrogen atoms, the compound is likely to be a solid or liquid at room temperature.

Explanation

The compound is expected to be stable under normal conditions, such as room temperature and pressure, due to the strong covalent bonds within its structure.

Explanation

The compound's amine group and phosphorus atom may react with strong acids, bases, or oxidizing agents, leading to changes in its chemical structure or properties.

Chemical structure

1,3-dimethyl-N,N-di(propan-2-yl)-1,3-dihydro-2H-1,3,2-benzodiazaphosphol-2-amine

Phosphazene compound

Yes

Industrial applications

Flame retardant, lubricant additive, precursor in the synthesis of other phosphorus-containing compounds

Structure

Contains a benzodiazaphosphol ring

Versatility

Potential uses in a variety of industries

Functional groups

Methyl, propyl, and amine groups

Physical state

Likely a solid or liquid at room temperature

Stability

Stable under normal conditions

Reactivity

May react with strong acids, bases, or oxidizing agents

Check Digit Verification of cas no

The CAS Registry Mumber 79607-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,0 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79607-90:
(7*7)+(6*9)+(5*6)+(4*0)+(3*7)+(2*9)+(1*0)=172
172 % 10 = 2
So 79607-90-2 is a valid CAS Registry Number.

79607-90-2SDS

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 1,3-dimethyl-N,N-di(propan-2-yl)-1,3,2-benzodiazaphosphol-2-amine

1.2 Other means of identification

Product number -
Other names 1H-1,3,2-Benzodiazaphosphole,2-diisopropylamino-1,3-dimethyl-2,3-dihydro

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:79607-90-2 SDS

79607-90-2Downstream Products

79607-90-2Relevant academic research and scientific papers

Conformation and Stereodynamics of 2-Dialkylamino-1,3-dimethyl-2,3-dihydro-1H-1,3,2-benzodiazaphospholes. An Experimental Nuclear Magnetic Resonance, Ultraviolet Photoelectron, and Theoretical MNDO Investigation

Jennings, W. Brian,Randall, David,Worley, S. Davis,Hargis, J. Howard

, p. 1411 - 1416 (2007/10/02)

Conformational information on the title compounds obtained from low temperature (13)C and (1)H n.m.r. studies is in agreement with the geometry calculated by the MNDO SCF molecular orbital procedure.The barriers to rotation about the exocyclic P-N bond have been measured and the rotational transition state has been investigated by MNDO.Some u.v. photoelectron and (15)N n.m.r. data are reported and the possibility of enhanced ?-bonding in the exocyclic PN bond is discussed.

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