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methyl 2-(phenylamino)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

121877-02-9

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121877-02-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121877-02-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,8,7 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 121877-02:
(8*1)+(7*2)+(6*1)+(5*8)+(4*7)+(3*7)+(2*0)+(1*2)=119
119 % 10 = 9
So 121877-02-9 is a valid CAS Registry Number.

121877-02-9Relevant academic research and scientific papers

Reaction of methyl diazoacetate with aldehydes, amines, thiols, alcohols and acids over transition metal-exchanged clays

Phukan, Prodeep,Mohan, Jakkam Madan,Sudalai, Arumugam

, p. 3685 - 3689 (1999)

Metal-exchanged clays (M = Rh and Cu) catalyze effectively the reaction of methyl diazoacetate with various aldehydes, affording the corresponding β-keto esters in high yields. They have also been effective in the decomposition of methyl diazoacetate to form metallocarbenes which, in turn, successfully insert into X-H (X = N, O, S, CO2) bonds of a variety of amines, aldehydes, thiols and acids, thereby producing the corresponding esters. The Royal Society of Chemistry 1999.

Thermolysis of polyazapentadienes. Part 10. Flash vacuum pyrolysis of azoalkenes and some azocarbonyl compounds

McNab, Hamish,Murray, M. Elizabeth-Ann

, p. 583 - 587 (2007/10/02)

Thermolysis of the azoalkenes (1) and (6) - (8) takes place by 4π-electron electrocyclisation, followed by elimination of HCN to give imines. Decomposition of the related compounds (9)-(12) is less well defined, though the indole (22) has been identified from the thermolysis of (10) at high temperature. Alternatively, the azo ketones (15) - (18) undergo homolysis of the central C-N bond at 750 °C, and low yields of biaryls, formed by intermolecular radical coupling are generally found. Decarbonylation of intermediate aroyl radicals is extremely rapid under these conditions.

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