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133891-59-5

133891-59-5

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133891-59-5 Usage

General Description

1-(DIPHENYLMETHYL)-3-METHYL-3-AZETIDINEMETHANAMINE is a chemical compound with a complex molecular structure. It is a type of azetidinamine, which is a class of compounds used in the pharmaceutical industry for their potential therapeutic applications. This particular compound contains a diphenylmethyl group and a methyl group, as well as an azetidinemethanamine moiety. The combination of these functional groups gives the compound unique chemical properties and potential biological activities. Further research and studies would be necessary to fully understand the potential uses and effects of 1-(DIPHENYLMETHYL)-3-METHYL-3-AZETIDINEMETHANAMINE.

Check Digit Verification of cas no

The CAS Registry Mumber 133891-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,8,9 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 133891-59:
(8*1)+(7*3)+(6*3)+(5*8)+(4*9)+(3*1)+(2*5)+(1*9)=145
145 % 10 = 5
So 133891-59-5 is a valid CAS Registry Number.

133891-59-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-benzhydryl-3-methylazetidin-3-yl)methanamine

1.2 Other means of identification

Product number -
Other names 3-aminomethyl-1-diphenylmethyl-3-methylazetidine

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:133891-59-5 SDS

133891-59-5Relevant articles and documents

The synthesis and biological evaluation of novel series of nitrile-containing fluoroquinolones as antibacterial agents

Murphy, Sean T.,Case, Heather L.,Ellsworth, Edmund,Hagen, Susan,Huband, Michael,Joannides, Themis,Limberakis, Chris,Marotti, Keith R.,Ottolini, Amy M.,Rauckhorst, Mark,Starr, Jeremy,Stier, Michael,Taylor, Clarke,Zhu, Tong,Blaser, Adrian,Denny, William A.,Lu, Guo-Liang,Smaill, Jeff B.,Rivault, Freddy

, p. 2150 - 2155 (2008/02/02)

Several novel series of nitrile-containing fluoroquinolones with weakly basic amines are reported which have reduced potential for hERG (human ether-a-go-go gene) channel inhibition as measured by the dofetilide assay. The new fluoroquinolones are potent

7-Azetidinylquinolones as antibacterial agents. Synthesis and structure- activity relationships

Frigola,Pares,Corbera,Vano,Merce,Torrens,Mas,Valenti

, p. 801 - 810 (2007/10/02)

A series of novel antibacterial quinolones and naphthyridones has been prepared which contain 7-azetidinyl substituents in place of the usual piperazine or aminopyrrolidine groups. These azetidinyl derivatives were evaluated for in vitro activity by deter

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