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Benzylammonium-trifluormethansulfonat is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105754-29-8

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105754-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105754-29-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,7,5 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105754-29:
(8*1)+(7*0)+(6*5)+(5*7)+(4*5)+(3*4)+(2*2)+(1*9)=118
118 % 10 = 8
So 105754-29-8 is a valid CAS Registry Number.

105754-29-8Relevant academic research and scientific papers

Green radicals of potassium poly(heptazine imide) using light and benzylamine

Markushyna, Yevheniia,Lamagni, Paolo,Teutloff, Christian,Catalano, Jacopo,Lock, Nina,Zhang, Guigang,Antonietti, Markus,Savateev, Aleksandr

, p. 24771 - 24775 (2019)

Tinted long-lived ionic carbon nitride radicals were recently introduced and applied in photocatalysis and energy storage. However, the reason for their higher activity in the photocatalytic reaction and optimal conditions for generating such radicals remain vague. Herein, we study the conditions for carbon nitride photocharging to achieve a higher charge density and validate a convenient method to quantify the number of electrons accumulated in carbon nitride semiconductors by quenching its radicals with methylviologen in the dark. In the presence of CO2, potassium poly(heptazine imide) (K-PHI) can be charged by up to 1000 μmol of electrons per gram of the material using benzylamine as an electron donor. Under the same conditions, mesoporous graphitic carbon nitride can accumulate only 50 μmol of electrons per gram. The products of the benzylamine oxidative coupling are imine and ammonia.

Amino Acids, 4 - Enantioselective Synthesis of N-Substituted α-Amino Carboxylic Acids from α-Hydroxy Carboxylic Acids

Effenberger, Franz,Burkard, Ulrike,Willfahrt, Joachim

, p. 314 - 333 (2007/10/02)

With primary and secondary amines, the (S)-α-(trifluoromethylsulfonyloxy) carboxylates (S)-3 afford in an SN2 reaction the N-substituted (R)-α-amino carboxylates (R)-5, (R)-9, and (R)-12, resp.The rates of α-substituted ethyl propionates decrease in the order of the substituents triflate (3a) >> bromide (8a) > mesylate (7a) >= tosylate (7b) > chloride (8b); in the reactions with amines, decreasing reactivity affords increasing racemisation and elimination as a consequence of the more drastic conditions which are required

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