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1088565-34-7

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1088565-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1088565-34-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,8,5,6 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1088565-34:
(9*1)+(8*0)+(7*8)+(6*8)+(5*5)+(4*6)+(3*5)+(2*3)+(1*4)=187
187 % 10 = 7
So 1088565-34-7 is a valid CAS Registry Number.

1088565-34-7Downstream Products

1088565-34-7Relevant academic research and scientific papers

Coupling of aldehydes, amines, and trimethyl phosphite promoted by amberlyst-15: Highly efficient synthesis of α-aminophosphonates

Tajbakhsh, Mahmood,Heydari, Akbar,Alinezhad, Heshmatollah,Ghanei, Mercedeh,Khaksar, Samad

, p. 352 - 354 (2008)

A three-component reaction promoted by Amberlyst-15 of an amine, an aldehyde, and trimethyl phosphite (Kabachnik-Fields reaction) in one pot under mild conditions affords the corresponding α-aminophosphonate in high yield after a short reaction time at ambient temperature. Georg Thieme Verlag Stuttgart.

A sulfonic acid functionalized ionic liquid as a homogeneous and recyclable catalyst for the one-pot synthesis of α-aminophosphonates

Akbari, Jafar,Heydari, Akbar

experimental part, p. 4236 - 4238 (2009/10/26)

A sulfonic acid functionalized ionic liquid is used as a Br?nsted acid catalyst for the one-pot, three-component synthesis of α-aminophosphonates from aldehydes and ketones at room temperature in water. This homogeneous catalytic procedure is simple and e

Organocatalytic synthesis of α-hydroxy and α-aminophosphonates

Vahdat, Seyed Mohammad,Baharfar, Robabeh,Tajbakhsh, Mahmood,Heydari, Akbar,Baghbanian, Seyed Meysam,Khaksar, Samad

scheme or table, p. 6501 - 6504 (2009/04/06)

A new and highly flexible procedure is described for the synthesis of α-amino- and α-hydroxy phosphonates. In the presence of a catalytic amount of oxalic acid (10 mol %), trimethyl phosphite reacts with aldehydes or imines (generated in situ from an aldehyde and an amine) to yield the corresponding coupled products in good yield.

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