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148278-90-4

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148278-90-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148278-90-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,2,7 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 148278-90:
(8*1)+(7*4)+(6*8)+(5*2)+(4*7)+(3*8)+(2*9)+(1*0)=164
164 % 10 = 4
So 148278-90-4 is a valid CAS Registry Number.

148278-90-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(methoxymethyl)phenyl]methanamine

1.2 Other means of identification

Product number -
Other names (3-(Methoxymethyl)phenyl)methanamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:148278-90-4 SDS

148278-90-4Downstream Products

148278-90-4Relevant articles and documents

NCO-chelated organoantimony(III) and organobismuth(III) dichlorides: Syntheses and structures

Vrana, Jan,Jambor, Roman,Ruzicka, Ales,Holecek, Jaroslav,Dostal, Libor

, p. 1041 - 1050 (2010)

The novel NCO chelating ligand L, 1-CH2N(CH3) 2-3-CH2OCH3-C6H4, was prepared in four steps from commercially available m-tolunitrile in a good yield. Successful lithiation of this ligand was achieved by the reaction with n-BuLi in hexane. Using of this in situ prepared organolithium compound LLi in the reactions with MCl3 (M = Sb, Bi) in 1:1 molar ratio led to isolation of the desired mono-organocompounds MLCl2 (M = Sb (1), Bi (2)). Their structures were studied both in solution (NMR) and in the solid state (X-ray diffraction), and were compared with those of the NCN- and OCO-chelating analogues.

COMPOUNDS WHICH INHIBIT BETA-SECRETASE ACTIVITY AND METHODS OF USE THEREOF

-

Page/Page column 54-55, (2008/06/13)

The present invention provides novel beta-secretase inhibitors of the general formula (I), where the variables A1, A2, L1, L2, L3, R1, R2, R3, R4, R5, R6 and R7 are as defined in the claims, a method for their use in treating Alzheimer's disease, and methods for their use in reducing memapsin 2 catalytic activity.

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