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4928-43-2

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4928-43-2 Usage

General Description

N2, N2-dimethylpyridine-2,5-diamine is a chemical compound that belongs to the class of compounds known as meta-aminophenols. These are organic polycyclic compounds that contain a benzene ring with two adjacent carbon atoms each bearing an amino group (-NH2). It also features two linked methyl groups (-CH3). The chemical formula for N2, N2-dimethylpyridine-2,5-diamine is C7H11N3, and it is often used in the synthesis of various organic compounds in the field of pharmaceuticals and biochemistry. The chemical possesses a strong nucleophilic property, meaning that it has the capacity to donate electron pairs to other compounds, a feature that makes it useful in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 4928-43-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,2 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4928-43:
(6*4)+(5*9)+(4*2)+(3*8)+(2*4)+(1*3)=112
112 % 10 = 2
So 4928-43-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H11N3/c1-10(2)7-4-3-6(8)5-9-7/h3-5H,8H2,1-2H3

4928-43-2Relevant articles and documents

COMPOUNDS TARGETING RNA-BINDING PROTEINS OR RNA-MODIFYING PROTEINS

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, (2021/09/11)

The invention relates to a compound represented by Formula (I): or a pharmaceutically acceptable salt thereof, compositions comprising the same and methods of preparing and using the same. The variables are described herein.

Discovery of potent transient receptor potential vanilloid 1 antagonists: Design and synthesis of phenoxyacetamide derivatives

Takahashi, Eiki,Hirano, Noriyuki,Nagahara, Takashi,Yoshikawa, Satoru,Momen, Shinobu,Yokokawa, Hiroshi,Hayashi, Ryoji

, p. 3154 - 3156 (2013/06/26)

We aimed to discover a novel type of transient receptor potential vanilloid 1 (TRPV1) antagonist because such antagonists are possible drug candidates for treating various disorders. We modified the structure of hit compound 7 (human TRPV1 IC50 = 411 nM) and converted its pyrrolidino group to a (hydroxyethyl)methylamino group, which substantially improved inhibitory activity (15d; human TRPV1 IC50 = 33 nM). In addition, 15d ameliorated bladder overactivity in rats in vivo.

SUBSTITUTED DIARYLAMINES AND USE OF SAME AS ANTIOXIDANTS

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, (2013/02/28)

The present invention relates to substituted heteroaromatic dianlamine compounds of Formula I and II, their pharmaceutically acceptable salts, and compositions thereof useful as antioxidants, wherein each of X, Y and Z are independently a carbon or nitrogen atom; R1 and R2 are each independently a hydrogen or an electron donating group, but are not both hydrogen, and wherein R1 and R2 are each bonded to a carbon atom in their own respective aryl ring.

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