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40398-28-5

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40398-28-5 Usage

General Description

(Morpholin-4-yl-carbothioyl)carbamic acid ethyl ester is an organic compound that is commonly used in the synthesis of various pharmaceuticals and agrochemicals. It is also known for its use as a reagent in organic chemistry reactions. This chemical is an ethyl ester derivative of carbamic acid, containing a morpholine ring and a carbothioyl group. It is utilized in the production of carbamates, which are used as pesticides and herbicides. Additionally, (morpholin-4-yl-carbothioyl)carbamic acid ethyl ester has potential applications in the development of novel drugs and materials due to its unique structure and reactivity. Overall, this compound is important in both the pharmaceutical and agricultural industries and has significant potential for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 40398-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,9 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40398-28:
(7*4)+(6*0)+(5*3)+(4*9)+(3*8)+(2*2)+(1*8)=115
115 % 10 = 5
So 40398-28-5 is a valid CAS Registry Number.

40398-28-5Relevant articles and documents

Reactivity of 1,2,3-triazole-substituted 1-azabutadienes (vinamidines)

Batori, Sandor,Bokotey, Sandor,Messmer, Andras

, p. 146 - 162 (2013/09/24)

The reactivity of the new 1,2,3-triazole-substituted vinamidines (i.e. 1-azabutadienes) was investigated. They were used as synthons to obtain new pyrazole, di-1,2,3-triazole as well as 4-amino-1,2,3-triazole derivatives. The Diels-Alder reaction with inverse electronic demand (using dimethyl 1,2,4,5-tetrazin-3,6-dicarboxylate as reagent) resulted in the formation of a new pyridazine derivative. ARKAT-USA Inc.

PEPTIDIC COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS

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Page 83-84, (2010/11/30)

The present invention is directed to compounds that are inhibitors of cysteine proteases, in particular, cathepsins B, K, L, F, and S and are therefore useful in treating diseases mediated by these proteases. The present invention is directed to pharmaceutical compositions comprising these compounds and processes for preparing them.

Novel compounds useful as reversible inhibitors of cysteine proteases

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, (2008/06/13)

Disclosed are novel cathepsin S, K, F, L and B reversible inhibitory compounds of the formula (Ia) and (Ib) where R2, R3, R4, R5, R6, R7, R8, Het and X are defined herein. The co

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