1401773-94-1

Basic information

• Product Name: (E)-3-(1-{4-[3-(2-pyridin-2-ylvinyl)phenylamino]phenyl}-1H-[1,2,3]triazol-4-yl)propan-1-ol
• Synonyms: (E)-3-(1-{4-[3-(2-pyridin-2-ylvinyl)phenylamino]phenyl}-1H-[1,2,3]triazol-4-yl)propan-1-ol
• CAS NO: 1401773-94-1
• Molecular Weight: 397.48
• Mol File: 1401773-94-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-3-(1-{4-[3-(2-pyridin-2-ylvinyl)phenylamino]phenyl}-1H-[1,2,3]triazol-4-yl)propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-(1-{4-[3-(2-pyridin-2-ylvinyl)phenylamino]phenyl}-1H-[1,2,3]triazol-4-yl)propan-1-ol(1401773-94-1)
• EPA Substance Registry System: (E)-3-(1-{4-[3-(2-pyridin-2-ylvinyl)phenylamino]phenyl}-1H-[1,2,3]triazol-4-yl)propan-1-ol(1401773-94-1)

Safety Data

• Hazardous Substances Data: 1401773-94-1(Hazardous Substances Data)

Upstream product

• 55532-26-8 (E)-2-(3-nitrostyryl)pyridine 
• 100-69-6 2-vinylpyridine 
• 585-79-5 m-nitrobromobenzene 
• 1401774-24-0 4-bromo-(4-(3-hydroxypropyl)-1H-1,2,3-triazol-1-yl)benzene 
• 176034-12-1 3-(trans-2-[2]pyridyl-vinyl)-aniline 
• 5390-04-5 pent-1-yn-5-ol 
• 589-87-7 1,4-bromoiodobenzene 
• 1379771-11-5 N-[2-(1-methoxybut-3-ynyl)phenyl]-4-nitrobenzenesulfonamide 

Relevant articles and documents

The structure-activity relationships of L3MBTL3 inhibitors: Flexibility of the dimer interface

We recently reported the discovery of UNC1215, a potent and selective chemical probe for the L3MBTL3 methyllysine reader domain. In this article, we describe the development of structure-activity relationships (SAR) of a second series of potent L3MBTL3 antagonists which evolved from the structure of the chemical probe UNC1215. These compounds are selective for L3MBTL3 against a panel of methyllysine reader proteins, particularly the related MBT family proteins, L3MBTL1 and MBTD1. A co-crystal structure of L3MBTL3 and one of the most potent compounds suggests that the L3MBTL3 dimer rotates about the dimer interface to accommodate ligand binding.

One-point binding ligands for asymmetric gold catalysis: Phosphoramidites with a TADDOL-related but acyclic backbone

Readily available phosphoramidites incorporating TADDOL-related diols with an acyclic backbone turned out to be excellent ligands for asymmetric gold catalysis, allowing a number of mechanistically different transformations to be performed with good to outstanding enantioselectivities. This includes [2 + 2] and [4 + 2] cycloadditions of ene-allenes, cycloisomerizations of enynes, hydroarylation reactions with formation of indolines, as well as intramolecular hydroaminations and hydroalkoxylations of allenes. Their preparative relevance is underscored by an application to an efficient synthesis of the antidepressive drug candidate (-)-GSK 1360707. The distinctive design element of the new ligands is their acyclic dimethyl ether backbone in lieu of the (isopropylidene) acetal moiety characteristic for traditional TADDOLs. Crystallographic data in combination with computational studies allow the efficiency of the gold complexes endowed with such one-point binding ligands to be rationalized.