182921-01-3

Basic information

• Product Name: Carbamic acid, [2-[4-(phenylmethoxy)phenyl]ethyl]-, 1,1-dimethylethyl ester
• CAS NO: 182921-01-3
• Molecular Formula: C20H25NO3
• Molecular Weight: 327.423
• Mol File: 182921-01-3.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [2-[4-(phenylmethoxy)phenyl]ethyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [2-[4-(phenylmethoxy)phenyl]ethyl]-, 1,1-dimethylethyl ester(182921-01-3)
• EPA Substance Registry System: Carbamic acid, [2-[4-(phenylmethoxy)phenyl]ethyl]-, 1,1-dimethylethyl ester(182921-01-3)

Safety Data

• Hazardous Substances Data: 182921-01-3(Hazardous Substances Data)

Upstream product

• 64318-28-1 N-t-butoxycarbonyl-tyramine 
• 100-39-0 benzyl bromide 
• 51-67-2 tyrosamine 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 788824-85-1 N-t-butoxycarbonyl-N-methyl-O-benzyltyramine 
• 788824-87-3 N-t-butoxycarbonyl-N-ethyl-O-benzyltyramine 
• 788824-90-8 N-t-butoxycarbonyl-N-benzyl-O-benzyltyramine 
• 51179-05-6 2-(4-(benzyloxy)phenyl)ethanamine 
• 1268607-25-5 [2-(4-benzyloxyphenyl)-ethyl]-pteridin-4-yl-amine 
• 1415684-17-1 (2S,3R,3aS,12bR)-1,2,3,3a,4,5,7,8-octahydro-11-benzyloxy-2-methyl-5-oxo-cyclopenta[2,3]pyrrolo[2,1-a]isoquinoline-3-carboxylic acid 
• 1415684-16-0 (2S,3R,3aS,12bR)-1,2,3,3a,4,5,7,8-octahydro-11-benzyloxy-2-methyl-3-nitromethyl-5-oxo-cyclopenta[2,3]pyrrolo[2,1-a]isoquinoline 
• 64318-28-1 N-t-butoxycarbonyl-tyramine 
• 182921-02-4 N-t-butoxycarbonyl-N-allyl-2-[(4-benzyloxy)-phenyl]-ethylamine 
• 24958-41-6 N-methyl-O-benzyltyramine hydochloride 
• 32293-43-9 N,O-dibenzyltyramine hydrochloride 
• 788824-88-4 N-t-butoxycarbonyl-N-propyl-O-benzyltyramine 
• 788824-89-5 N-t-butoxycarbonyl-N-butyl-O-benzyltyramine 

Relevant articles and documents

Guanidinium compounds with sub-micromolar activities against Mycobacterium tuberculosis. Synthesis, characterization and biological evaluations

Seven polycharged species, incorporating 1, 2, 3, 4 and 6 guanidine arms organized around a benzene core were synthesized and assayed as anti-mycobacterial agents against Mycobacterium tuberculosis. They display MIC values comprised between 25 and 12.5 μM (close to ethambutol EMB) for the mono- and the hexa-substituted derivatives, and 0.8 μM (close to isoniazid and streptomycin) for the tri-substituted derivative. The three bi- and the tetra-substituted analogs displayed MIC values of ca. 6.5-3.0 μM. The latter were also evaluated against the isoniazid-resistant MYC5165 strain, resulting in highly interesting micromolar or sub-micromolar MIC, ca. 4-125 times more active than isoniazid. These preliminary results are attractive for the development of new anti-TB agents.

Diverse alkaloid-like structures from a common building block

A wealth of unique enantiopure polycyclic alkaloid-like scaffolds can be prepared on a multigram scale in only a few steps from a common, commercially available intermediate. The attached nitromethyl group can then be used to construct highly diverse func

PTERIDINES AND THEIR USE AS AGROCHEMICALS

The present disclosure relates to 1- or 2-(4-(aryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and 1- or 2-(4-(heteroaryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and their use as agrochemicals and animal health products.