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24422-55-7

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24422-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24422-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,2 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24422-55:
(7*2)+(6*4)+(5*4)+(4*2)+(3*2)+(2*5)+(1*5)=87
87 % 10 = 7
So 24422-55-7 is a valid CAS Registry Number.

24422-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-diphenylphosphoryl-N,N-dimethylethanamine

1.2 Other means of identification

Product number -
Other names HMS2625L08

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:24422-55-7 SDS

24422-55-7Relevant articles and documents

Crystal and molecular structure of [(C6H5)2P(=O)(CH2CH 2N(CH3)3)+][I-]

Churchill, Melvyn Rowen,See, Ronald F.,Rominger, Robert L.,Atwood, Jim D.

, p. 747 - 752 (1996)

The title compound crystallizes in the centrosymmetric triclinic space group Pl with Z = 4. The crystallographic asymmetric unit contains two independent cations; interatomic distances within these include P=O = 1.47(1) and 1.47(1)?, P-C6H

A practical and efficient green synthesis of β-aminophosphoryl compounds via the aza-Michael reaction in water

Matveeva, Ekaterina V.,Petrovskii, Pavel V.,Klemenkova, Zinaida S.,Bondarenko, Natalya A.,Odinets, Irina L.

experimental part, p. 964 - 970 (2011/11/05)

Biphasic systems room temperature imidazolium ionic liquid (RTIL)/water or water as a solvent significantly accelerate the addition of amines to vinylphosphoryl compounds hence opening green and effective synthesis of β-aminophosphoryl compounds in excellent yields over short reaction times. The application of water, being the cheapest and most non-toxic solvent, without any catalyst or co-solvent, is more advantageous as it provides a simple isolation procedure for products having high purity (> 95% according to the NMR data) via simple freeze-drying and does not require extraction with organic solvents. The solubility of the starting phosphorus substrate in water does not play crucial role in the reaction as it was demonstrated using water insoluble diphenylvinylphosphine oxide. In contrast to typical procedures, using a reactant ratio (vinylphosphoryl compound: amine) of 2:1 readily resulted in double phosphorylation of primary amines, including polyamines, in water.

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