58114-05-9

Basic information

• Product Name: Benzene, 1-(1-chloroethyl)-3-methoxy-
• CAS NO: 58114-05-9
• Molecular Formula: C9H11ClO
• Molecular Weight: 170.639
• Mol File: 58114-05-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(1-chloroethyl)-3-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(1-chloroethyl)-3-methoxy-(58114-05-9)
• EPA Substance Registry System: Benzene, 1-(1-chloroethyl)-3-methoxy-(58114-05-9)

Safety Data

• Hazardous Substances Data: 58114-05-9(Hazardous Substances Data)

Upstream product

• 89691-63-4 1-(3-methoxy)-phenylethanol 
• 626-20-0 3-methoxystyrene 
• 586-37-8 1-(3-Methoxyphenyl)ethanone 
• 591-31-1 3-methoxy-benzaldehyde 

Downstream Products

• 89691-63-4 1-(3-methoxy)-phenylethanol 
• 626-20-0 3-methoxystyrene 
• 68266-29-5 3,3'-(butane-2,3-diyl)bis(methoxybenzene) 
• 865874-20-0 1-[1-(3-methoxy-phenyl)-ethyl]-pyrrolidine 
• 865874-23-3 4-[1-(3-methoxy-phenyl)-ethyl]-morpholine 
• 865874-24-4 1-[1-(3-methoxy-phenyl)-ethyl]-4-methyl-piperazine 
• 10568-38-4 3-ethylanisole 
• 68266-23-9 meso-2,3-bis(3'-hydroxyphenyl)butane 

Relevant articles and documents

Nickel-Catalyzed Multicomponent Coupling: Synthesis of α-Chiral Ketones by Reductive Hydrocarbonylation of Alkenes

A nickel-catalyzed, multicomponent regio- and enantioselective coupling via sequential hydroformylation and carbonylation from readily available starting materials has been developed. This modular multicomponent hydrofunctionalization strategy enables the straightforward reductive hydrocarbonylation of a broad range of unactivated alkenes to produce a wide variety of unsymmetrical dialkyl ketones bearing a functionalized α-stereocenter, including enantioenriched chiral α-aryl ketones and α-amino ketones. It uses chiral bisoxazoline as a ligand, silane as a reductant, chloroformate as a safe CO source, and a racemic secondary benzyl chloride or an N-hydroxyphthalimide (NHP) ester of a protected α-amino acid as the alkylation reagent. The benign nature of this process renders this method suitable for late-stage functionalization of complex molecules.

NOVEL 5-SUBSTITUTED 7-AMINO-[1,3]THIAZOLO[4,5-D]PYRIMIDINE DERIVATIVES

There are disclosed novel 5-substituted 7-amino-[1,3]thiazolo[4,5-d]pyrimidine derivatives of formula (I) wherein R1, R2, R3, R4 and R5 are as defined in the specification, and pharmaceutically accept

Novel di-(3'-hydroxyphenyl)-alkane compounds, process of preparation and their use in medicine

Compounds of di-(3'-hydroxyphenyl)-alkanes and their methyl ethers, of the formula STR1 wherein R is alkyl and R' is H or methyl, have activity against hormone-dependent breast carcinoma.