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35155-84-1

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35155-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35155-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,5 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35155-84:
(7*3)+(6*5)+(5*1)+(4*5)+(3*5)+(2*8)+(1*4)=111
111 % 10 = 1
So 35155-84-1 is a valid CAS Registry Number.

35155-84-1Relevant articles and documents

How Water in Aliphatic Solvents Directs the Interference of Chemical Reactivity in a Supramolecular System

Mabesoone, Mathijs F. J.,Ter Huurne, Gijs M.,Palmans, Anja R. A.,Meijer

, p. 12400 - 12408 (2020)

Water is typically considered to be insoluble in alkanes. Recently, however, monomerically dissolved water in alkanes has been shown to dramatically impact the structure of hydrogen-bonded supramolecular polymers. Here, we report that water in methylcyclo

The study of biocatalyzed thio-Michael reaction: A greener and multi-gram protocol

Rizzo, Paula V.S.,Boarin, Ligia A.,Freitas, Ingridhy O.M.,Gomes, Roberto S.,Beatriz, Adilson,Rinaldi, Andrelson W.,Domingues, Nelson Luís C.

, p. 430 - 434 (2014)

This Letter introduces a new, cheap and green protocol for the thio-Michael reaction. Here we applied three free enzymes such as lipase from pancreas porcine, chymosin and papain and an immobilized one: the Liposyme. The reactions were executed at room te

Method for synthesizing beta-thiocarbonyl compound by taking aryl sulfonyl chloride as sulfur source

-

Paragraph 0042; 0043; 0044; 0045, (2020/11/09)

The invention discloses a method for synthesizing a beta-thiocarbonyl compound by taking aryl sulfonyl chloride as a sulfur source, comprising the following steps of: in an air atmosphere, adding arylsulfonyl chloride, ketene, triphenylphosphine, potassiu

Thioboration of α,β-unsaturated ketones and aldehydes toward the synthesis of β-sulfido carbonyl compounds

Civit, Marc G.,Sanz, Xavier,Vogels, Christopher M.,Webb, Jonathan D.,Geier, Stephen J.,Decken, Andreas,Bo, Carles,Westcott, Stephen A.,Fernández, Elena

, p. 2148 - 2154 (2015/05/19)

Herein a direct β-sulfido carbonyl compound synthesis by the easy activation of RS-Bpin reagents with α,β-unsaturated ketones and aldehydes is reported. This convenient methodology can be performed at room temperature with no other additives. The key poin

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