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O-methyl (4-methoxyphenyl)carbamothioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22007-37-0

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22007-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22007-37-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,0 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22007-37:
(7*2)+(6*2)+(5*0)+(4*0)+(3*7)+(2*3)+(1*7)=60
60 % 10 = 0
So 22007-37-0 is a valid CAS Registry Number.

22007-37-0Relevant academic research and scientific papers

A novel three-component reaction between isocyanides, alcohols or thiols and elemental sulfur: A mild, catalyst-free approach towards O-thiocarbamates and dithiocarbamates

Németh, András Gy?rgy,Keseru, Gy?rgy Miklós,ábrányi-Balogh, Péter

supporting information, p. 1523 - 1533 (2019/08/07)

A new multicomponent reaction has been developed between isocyanides, sulfur and alcohols or thiols under mild reaction conditions to afford O-thiocarbamates and dithiocarbamates in moderate to good yields. The one-pot reaction cascade involves the formation of an isothiocyanate intermediate, thus a catalyst-free synthesis of isothiocyanates, as valuable building blocks from isocyanides and sulfur is proposed, as well. The synthetic procedure suits the demand of a modern organic chemist, as it tolerates a wide range of functional groups, it is atom economic and easily scalable.

Glycosyl alkoxythioimidates as building blocks for glycosylation: A reactivity study

Ranade, Sneha C.,Demchenko, Alexei V.

, p. 115 - 122 (2015/02/19)

Structural modifications of the leaving group of S-glycosyl O-methyl phenylcarbamothioates (SNea) involving change of substituents that express different electronic effects led to a better understanding of how the reactivity of these glycosyl donors can b

REACTIONS OF 1-CHLOROALKYL ISOCYANATES WITH THIOURETHANES

Vovk, M. V.,Davidyuk, Yu. N.,Chernega, A. N.,Tsymbal, I. F.,Samarai, L. I.

, p. 1635 - 1643 (2007/10/02)

1-Chloroalkyl isocyanates react with thiourethanes to gives N-acylation products, namely, N-(N-alkylidenaminocarbonyl)thiourethanes, which exist in solution in tautomeric equilibrium with S-(1-isocyanatoalkyl)isothiourethanes.These tautomeric transformation occur in the C=N-C azaallylic system involving a new anionotropic migrant, namely, the thiocarbamyl group.The reactions of these tautomeric compounds with water, alcohols, phenol, and primary amines proceed with the participation of the azomethine form, while the reactions with secondary amines involve the isocyanate form.

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