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3-((tert-butoxycarbonyl)amino)propane-1,2-diyl dimethanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

213475-72-0

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213475-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 213475-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,4,7 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 213475-72:
(8*2)+(7*1)+(6*3)+(5*4)+(4*7)+(3*5)+(2*7)+(1*2)=120
120 % 10 = 0
So 213475-72-0 is a valid CAS Registry Number.

213475-72-0Relevant academic research and scientific papers

Convenient and simplified approaches to w-monoprotected triaminopropane derivatives: Key intermediates for bifunctional chelating agent synthesis

Benoist, Eric,Loussouarn, Anthony,Remaud, Patricia,Chatal, Jean-Francois,Gestin, Jean-Francois

, p. 1113 - 1118 (1998)

High yields of selectively Ar-protected-1,2,3-triaminopropanes (1,3 or 1,2 functionalized diamines) were obtained in 6 or 4 steps from diamino alcohols or aminodiols, respectively. These two multi-step procedures involve protection of the amino group, substitution of the hydroxy group by an azido group and selective reduction. The conditions for the first procedure allow the preparation of various Af2-monoprotected-l,2,3-triaminopropanes 6a, 6b, but the second one is more convenient for obtaining N1-Boc-1,2,3-triaminopropane 6'. These two simplified procedures, which provide functionalized 1,2 or 1,3 diamines easily and with good overall yields, could be useful for the synthesis of : bifunctional chelating agents.

SULFONIMIDAMIDE COMPOUNDS AS NLRP3 MODULATORS

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Paragraph 1362, (2021/07/31)

Described herein are compounds of Formula (I), Formula (I-A), and Formula (I-B), solvates thereof, tautomers thereof, and pharmaceutically acceptable salts of the foregoing, Further described herein are methods of inhibiting NLRP3 using said compounds, and methods of and compositions useful in treating NLRP3-dependent disorders.

Synthesis and pharmacological characterization of constrained analogues of Vestipitant as in vitro potent and orally active NK1 receptor antagonists

Sabbatini, Fabio M.,Fabio, Romano Di,Griffante, Cristiana,Pentassuglia, Giorgio,Zonzini, Laura,Melotto, Sergio,Alvaro, Giuseppe,Capelli, Anna M.,Pippo, Lara,Perdona', Elisabetta,Denis, Yves St.,Costa, Silvano,Corsi, Mauro

scheme or table, p. 623 - 627 (2010/06/12)

A focused exploration targeting conformationally restricted analogues of Vestipitant, resulted in the discovery of novel, in vitro potent NK1 antagonists. In particular, two of the compounds reported exhibited a good pharmacokinetic (PK) profile and produced anxiolytic-like effects in the gerbil foot tapping (GFT) in vivo model.

Synthesis and properties of diazirinyl organo-platinum compounds for manipulations of photoaffinity labeled components

Hashimoto, Makoto,Furukawa, Keitaro,Tomohiro, Takenori,Hatanaka, Yasumaru

scheme or table, p. 405 - 407 (2011/02/28)

Synthesis of diazirinyl organo-platinum complexes, which specifically interact with purine base, characterization of photoreactivity and interaction between guanosine 5′-monophosphate (GMP) were examined. The results indicated that the diazirinyl organo-platinum complex was useful for manipulations of photoaffinity labeled components.

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