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diethylammonium bis[2-(4-methoxyphenyl)ethyl]thioselenophosphinate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1259008-99-5

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1259008-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1259008-99-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,9,0,0 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1259008-99:
(9*1)+(8*2)+(7*5)+(6*9)+(5*0)+(4*0)+(3*8)+(2*9)+(1*9)=165
165 % 10 = 5
So 1259008-99-5 is a valid CAS Registry Number.

1259008-99-5Downstream Products

1259008-99-5Relevant academic research and scientific papers

Novel atom-economic synthesis of thioselenophosphinates via three-component reaction between secondary phosphine sulfides, elemental selenium, and amines

Artem'Ev, Alexander V.,Malysheva, Svetlana F.,Korocheva, Anastasiya O.,Gatilov, Yuriy V.,Mamatyuk, Victor I.,Gusarova, Nina K.

experimental part, p. 599 - 610 (2012/05/04)

An efficient, general, and atom-economic synthesis of organoammonium thioselenophosphinates has been developed by exploiting a three-component reaction between secondary phosphine sulfides, elemental selenium, and various amines. The reaction proceeds und

One-pot atom-economic synthesis of thioselenophosphinates via a new multicomponent reaction of secondary phosphanes with elemental sulfur, selenium, and amines

Artem'Ev, Alexander V.,Gusarova, Nina K.,Malysheva, Svetlana F.,Mamatyuk, Victor I.,Gatilov, Yurii V.,Ushakov, Igor A.,Trofimov, Boris A.

supporting information; experimental part, p. 6157 - 6160 (2010/12/29)

The multicomponent reaction between secondary phosphanes R2PH (R = Ph, arylalkyl, hetarylalkyl), elemental sulfur, selenium, and primary, secondary, or tertiary amines to afford the corresponding mono-, di-, and trialkylammonium thioselenophosphinates has been discovered. The atom-economic reaction proceeds under mild conditions (ethanol/toluene, 40-70 °C, 40 min) to give the target alkylammonium thioselenophosphinates in high yields (up to 94%). A family of hitherto unknown mono-, di-, and trialkylammonium thioselenophosphinates has been synthesized in high yields under mild conditions through a novelmulticomponent atom-economic reaction between secondary phosphanes, elemental sulfur, selenium, and primary, secondary, or tertiary amines.

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