2202-65-5

Basic information

• Product Name: Benzeneethanol, b-(dimethylamino)-, (R)-
• CAS NO: 2202-65-5
• Molecular Formula: C10H15NO
• Molecular Weight: 165.235
• Mol File: 2202-65-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzeneethanol, b-(dimethylamino)-, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneethanol, b-(dimethylamino)-, (R)-(2202-65-5)
• EPA Substance Registry System: Benzeneethanol, b-(dimethylamino)-, (R)-(2202-65-5)

Safety Data

• Hazardous Substances Data: 2202-65-5(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 56613-80-0 D-2-phenylglycinol 
• 29810-09-1 (R)-2-(dimethylamino)-2-phenylacetic acid 

Downstream Products

• 74492-08-3 (R)-phenyl-glyphos 
• 2202-68-8 (S)-2-dimethylamino-1-phenylethanol 
• 34469-09-5 (R)-2-dimethylamino-1-phenyl-ethanol 
• 2202-63-3 ((R)-2-Chloro-1-phenyl-ethyl)-dimethyl-amine; hydrochloride 

Relevant articles and documents

Highly efficient helix-sense-selective polymerization of an achiral phenylacetylene having a bulky group

Novel achiral phenylacetylene having a bulky t-butyl group was synthesized and polymerized by a chiral catalytic system containing [Rh(nbd)Cl]2 (nbd: norbornadiene) and chiral amines to yield a one-handed helical polymer having a much higher g value than polymers with no bulky groups. Highly efficient helix-sense-selective polymerization has been achieved using a bulky monomer and a less bulky chiral cocatalyst.

CARBONYLAMINO PYRROLOPYRAZOLES, POTENT KINASE INHIBITORS

Carbonylamino Pyrrolopyrazole compounds of formula I, compositions including these compounds and methods of their use are provided. Preferred compounds of formula I have activity as protein kinase inhibitors, including as inhibitors of PAK4.

Stevens Rearrangement of a Cyclic Hemiacetal System: Diastereoselective Approach to Chiral α-Amino Ketone

The base-promoted reaction of ammonium ylide 1a, which forms a cyclic hemiacetal structure, is shown to afford the anti-hemiacetal 3a in high diastereopurity, via the Stevens rearrangement followed by efficient thermodynamic epimerization.