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3-(4-methoxybenzyl)imidazolidine-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133886-13-2

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133886-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133886-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,8,8 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133886-13:
(8*1)+(7*3)+(6*3)+(5*8)+(4*8)+(3*6)+(2*1)+(1*3)=142
142 % 10 = 2
So 133886-13-2 is a valid CAS Registry Number.

133886-13-2Downstream Products

133886-13-2Relevant academic research and scientific papers

NOVEL AMIDE DERIVATIVE AND USE THEREOF AS MEDICINE

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Paragraph 0777; 0778; 0779, (2013/03/26)

Provided are a novel low-molecular-weight compound that suppresses production of induction type MMPs, particularly MMP-9, rather than production of hemostatic type MMP-2, as well as a prophylactic/therapeutic drug for autoimmune diseases or osteoarthritis. An amide derivative represented by the following formula (I) wherein each symbol is as defined in the specification, or a pharmacologically acceptable salt thereof.

BIFUNCTIONAL HETEROCYCLIC COMPOUNDS AND METHODS OF MAKING AND USING THE SAME

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Page 123, (2010/02/08)

The invention provides a family of bifunctional heterocyclic compounds useful as anti-infective, anti-proliferative, anti-inflammatory, and prokinetic agents. The invention also provides methods of making the bifunctional heterocyclic compounds, and metho

Synthetic studies on (+)-hydantocidin (1): A total synthesis of (+)-hydantocidin, a new herbicidal metabolite from microorganism

Mio, Shigeru,Ichinose, Reiji,Goto, Kuniko,Sugai, Soji,Sato, Sadao

, p. 2111 - 2120 (2007/10/02)

A total synthesis of (+)-hydantocidin 1, a new class of ribofuranose derivative exhibiting herbicidal activity, is reported. The spiro-hydantoin ring at the anomeric position of D-ribofuranose was constructed from substituted hydantoin derivatives 6, 7, and 12 through acid and base-promoted cyclization methods.

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