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N-(cyclopropylmethyl)-P,P-diphenylphosphinic amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68036-36-2

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68036-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68036-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,3 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 68036-36:
(7*6)+(6*8)+(5*0)+(4*3)+(3*6)+(2*3)+(1*6)=132
132 % 10 = 2
So 68036-36-2 is a valid CAS Registry Number.

68036-36-2Downstream Products

68036-36-2Relevant academic research and scientific papers

A practical method for N-alkylation of phosphinic (thio)amides with alcohols via transfer hydrogenation

Jankins, Tanner C.,Qin, Zi-Yang,Engle, Keary M.

, p. 3272 - 3281 (2019)

This manuscript describes a modular method for preparing N-alkyl phosphinic amides from primary or secondary alcohols and primary phosphinic amide (R1R2P = ONH2) nucleophiles via transfer hydrogenation. The transformation typically proceeds in excellent yields, employs conveniently available reagents, and produces water as the only byproduct.

Iridium Supported on Phosphorus-Doped Porous Organic Polymers: Active and Recyclable Catalyst for Acceptorless Dehydrogenation and Borrowing Hydrogen Reaction

Yao, Wei,Duan, Zheng-Chao,Zhang, Yilin,Sang, Xinxin,Xia, Xiao-Feng,Wang, Dawei

supporting information, p. 5695 - 5703 (2019/12/30)

Iridium-on-phosphorus-doped porous organic polymers (POP?Ir) were developed by anchoring simple iridium onto the skeleton of porous organic polymers through coordination bonds. This POP?Ir catalyst, which was thoroughly characterized by means of EDS, SEM, TEM, XRD, XPS, and FT-IR, revealed excellent catalytic activity for the reaction of diphenyl phosphinamide with benzyl alcohols through borrowing hydrogen strategy and acceptorless dehydrogenation with wide functional group tolerance. Moreover, this POP?Ir catalyst could be simply recovered and reused for at least five times without a significant loss of activity, and revealed considerable application prospects. The mechanism was investigated to further understand this POP?Ir catalytic system and transformations. Overall, the POP?Ir catalytic system has shown high activity and reusability in the borrowing hydrogen reaction between diphenyl phosphinamides and benzyl alcohols. (Figure presented.).

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