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(3R)-5-METHOXY-2,3-DIHYDRO-1-BENZOFURAN-3-AMINE is a chemical compound with the molecular formula C10H11NO2. It is a derivative of benzofuran, a heterocyclic compound found in some natural products and pharmaceuticals. (3R)-5-METHOXY-2,3-DIHYDRO-1-BENZOFURAN-3-AMINE contains a benzene ring fused to a furan ring and an amine functional group, and the 5-methoxy substituent indicates the presence of a methoxy group at the 5-position of the benzofuran ring. This chemical may have potential biological activities and pharmaceutical applications due to its unique structure and functional groups.

1228561-06-5

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1228561-06-5 Usage

Uses

Further research and investigation are needed to determine the specific properties and potential uses of (3R)-5-METHOXY-2,3-DIHYDRO-1-BENZOFURAN-3-AMINE.

Check Digit Verification of cas no

The CAS Registry Mumber 1228561-06-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,5,6 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1228561-06:
(9*1)+(8*2)+(7*2)+(6*8)+(5*5)+(4*6)+(3*1)+(2*0)+(1*6)=145
145 % 10 = 5
So 1228561-06-5 is a valid CAS Registry Number.

1228561-06-5Downstream Products

1228561-06-5Relevant academic research and scientific papers

Design and synthesis of dihydrobenzofuran amides as orally bioavailable, centrally active γ-secretase modulators

Pettersson, Martin,Johnson, Douglas S.,Subramanyam, Chakrapani,Bales, Kelly R.,Am Ende, Christopher W.,Fish, Benjamin A.,Green, Michael E.,Kauffman, Gregory W.,Lira, Ricardo,Mullins, Patrick B.,Navaratnam, Thayalan,Sakya, Subas M.,Stiff, Cory M.,Tran, Tuan P.,Vetelino, Beth C.,Xie, Longfei,Zhang, Liming,Pustilnik, Leslie R.,Wood, Kathleen M.,O'Donnell, Christopher J.

, p. 2906 - 2911 (2012/06/04)

We report the discovery and optimization of a novel series of dihydrobenzofuran amides as γ-secretase modulators (GSMs). Strategies for aligning in vitro potency with drug-like physicochemical properties and good microsomal stability while avoiding P-gp mediated efflux are discussed. Lead compounds such as 35 and 43 have moderate to good in vitro potency and excellent selectivity against Notch. Good oral bioavailability was achieved as well as robust brain Aβ42 lowering activity at 100 mg/kg po dose.

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