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42053-26-9

42053-26-9

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42053-26-9 Usage

Chemical Properties

DIETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE is Colourless Oil Which May Be Hazy

Uses

Different sources of media describe the Uses of 42053-26-9 differently. You can refer to the following data:
1. DIETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE is a useful reagent for the efficient phosphorylative conversion of alcohols into their corresponding diethyl phosphorotriesters. d=1.028
2. A useful reagent for the efficient phosphorylative conversion of alcohols into their corresponding diethyl phosphorotriesters.d=1.028

Check Digit Verification of cas no

The CAS Registry Mumber 42053-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,5 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42053-26:
(7*4)+(6*2)+(5*0)+(4*5)+(3*3)+(2*2)+(1*6)=79
79 % 10 = 9
So 42053-26-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H24NO2P/c1-7-12-14(13-8-2)11(9(3)4)10(5)6/h9-10H,7-8H2,1-6H3

42053-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-diethoxyphosphanyl-N-propan-2-ylpropan-2-amine

1.2 Other means of identification

Product number -
Other names N-diethoxyphosphanyl-N-propan-2-yl-propan-2-amine

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:42053-26-9 SDS

42053-26-9Relevant articles and documents

Phosphoric acid phaseomannite class compound and its preparation method and application (by machine translation)

-

, (2017/07/14)

The invention discloses a phaseomannite class phosphate compound, phosphoric acid phaseomannite class compound preparation method, and these phosphoric acid phaseomannite class compounds in the preparation of an anti-tumor drug. The use of non-small cell lung cancer cells to the compounds of this invention to inhibit the growth of tumor cells in active testing, that the compounds of this invention have high inhibition of tumor cell growth activity, some of the compound inhibiting activity even with cisplatin active quite, which indicates that the compounds of this invention have good cell penetrability and phosphorus esterase stability, can be used for the development of anti-tumor medicament. (by machine translation)

Synthesis of 1,2-Azaphosphetidines

Afarinkia, Kamyar,Cadogan, John I. G.,Rees, Charles W.

, p. 285 - 287 (2007/10/02)

Photolytic or rhodium catalysed decomposition of α-diazo-β-ketophosphonamidates and intramolecular C-H insertion of the resulting carbene intermediates is the key step in the synthesis of mono and bicyclic 1,2-azaphosphetidines.

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