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120838-62-2

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120838-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120838-62-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,8,3 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 120838-62:
(8*1)+(7*2)+(6*0)+(5*8)+(4*3)+(3*8)+(2*6)+(1*2)=112
112 % 10 = 2
So 120838-62-2 is a valid CAS Registry Number.

120838-62-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[3-(1-benzhydrylazetidin-3-yl)oxy-2-hydroxypropoxy]-1H-indole-2-carbonitrile

1.2 Other means of identification

Product number -
Other names Bdf-9148

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:120838-62-2 SDS

120838-62-2Downstream Products

120838-62-2Relevant articles and documents

New indolylpropanols, processes for their preparation and their use, and preparations containing the compounds

-

, (2008/06/13)

Substituted indolylpropanols of the formula I STR1 in which R1 denotes a cyano, carboxamido, alkoxycarbonyl, hydroxyl or acetyl group, Y stands for the group A STR2 wherein n is the number 2 or 3, or the group B, STR3 R2 stands for R2 ' where Y denotes the group A and for R2 " when Y denotes the group B, where R2 ' denotes pyridinyl, thienyl or substituted phenyl which is monosubstituted or disubstituted by difluoromethoxy, difluoromethylthio, trifluoromethoxy, trifluoromethylthio, trifluoroethoxy, alkoxyalkoxy, cycloalkylalkoxy, alkoxyalkyl, alkylthioalkoxy, alkylsulphinylalkoxy, alkylsulphonylalkoxy, alkoxyalkylthio, alkoxyalkylsulphinyl, alkoxyalkylsulphonyl, alkylthioalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl and dialkylaminoalkoxy, and R2 " denotes pyridinyl, thienyl, phenyl or substituted phenyl which is monosubstituted or disubstituted by halogen, alkyl, cycloalkyl, alkoxy, difluoromethoxy, difluoromethylthio, trifluoromethoxy, trifluoromethylthio, trifluoroethoxy, alkoxyalkoxy, cycloalkylalkoxy, alkoxyalkyl, alkylthioalkoxy, alkylsulphinylalkoxy, alkylsulphonylalkoxy, alkoxyalkylthio, alkoxyalkylsulphinyl, alkoxyalkylsulphonyl, alkylthioalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl and dialkylaminoalkoxy, and R3 stands for R3 ' when Y denotes the group A and for R3 " when R denotes the group B, where R3 ' denotes hydrogen, difluoromethoxy, difluoromethylthio, trifluoromethoxy, trifluoromethylthio, trifluoroethoxy, alkoxylalkoxy, alkoxyalkyl, alkylthioalkoxy, alkylsulphinylalkoxy, alkylsulphonylalkoxy, alkoxyalkylthio, alkoxyalkylsulphinyl, alkoxyalkylsulphonyl, alkylthioalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl or dialkylaminoalkoxy, and R3 " denotes hydrogen, alkoxy, halogen, difluoromethoxy, difluoromethylthio, trifluoromethoxy, trifluoromethylthio, trifluoroethoxy, alkoxyalkoxy, alkoxyalkyl, alkylthioalkoxy, alkylsulphinylalkoxy, alkylsulphonylalkoxy, alkoxyalkylthio, alkoxyalkylsulphinyl, alkoxyalkylsulphonyl, alkylthioalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl or dialkylaminoalkoxy, or a physiologically tolerable hydrolysable derivative thereof, in which the hydroxyl group in the 2-position of the 3-aminopropoxy side chain is present in esterified form, and also their tautomeric forms and their salts and also acid addition salts, where in all cases previously mentioned alkyl of the alkyl groups or of alkyl moieties or alkylene moieties of groups in each case denotes straight-chain or branched alkyl or alkylene having 1 to 6 carbon atoms and cycloalkyl has 3 to 7 carbon atoms, with the proviso that if R2 ' denotes pyridinyl or thienyl, R3 ' does not denote hydrogen, but one of the other R3 radicals mentioned show positive inotropic, vasodilatory and antiarrhythmic action and are suitable for the treatment of cardiac insufficiency, cardiac arrhythmias and hypertonia, coronary heart disease and peripheral and central arterial circulatory disturbances.

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