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1-(DIPHENYLMETHYL)-3-METHYL-3-AZETIDINEMETHANAMINE is a complex chemical compound belonging to the azetidinamine class, which is utilized in the pharmaceutical industry for its potential therapeutic applications. This specific compound features a diphenylmethyl group, a methyl group, and an azetidinemethanamine moiety, which together confer unique chemical properties and possible biological activities. Further research and studies are required to fully explore the potential uses and effects of this compound.

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  • 133891-59-5 Structure
  • Basic information

    1. Product Name: 1-(DIPHENYLMETHYL)-3-METHYL-3-AZETIDINEMETHANAMINE
    2. Synonyms: 1-(DIPHENYLMETHYL)-3-METHYL-3-AZETIDINEMETHANAMINE;(1-Benzhydryl-3-Methylazetidin-3-yl)MethanaMine;1-Benzhydryl-3-methyl-3-azetidinemethanamine
    3. CAS NO:133891-59-5
    4. Molecular Formula: C18H22N2
    5. Molecular Weight: 266.38
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133891-59-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C(protect from light)
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(DIPHENYLMETHYL)-3-METHYL-3-AZETIDINEMETHANAMINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(DIPHENYLMETHYL)-3-METHYL-3-AZETIDINEMETHANAMINE(133891-59-5)
    11. EPA Substance Registry System: 1-(DIPHENYLMETHYL)-3-METHYL-3-AZETIDINEMETHANAMINE(133891-59-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 133891-59-5(Hazardous Substances Data)

133891-59-5 Usage

Uses

Used in Pharmaceutical Industry:
1-(DIPHENYLMETHYL)-3-METHYL-3-AZETIDINEMETHANAMINE is used as a pharmaceutical compound for its potential therapeutic applications due to its unique molecular structure and functional groups. The specific combination of a diphenylmethyl group, a methyl group, and an azetidinemethanamine moiety may contribute to its potential biological activities and medicinal uses, although further research is needed to confirm these possibilities.

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

QUINOLONE ANTIBACTERIAL AGENTS

-

Page/Page column 85; 86, (2010/02/12)

Compounds of formula (I) wherein A is formula (II), formula (III) or formula (IV), and B is formula (V), formula (VI), or formula (VII), can be used in a variety of applications including use as antibacterial agents.

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

Substituted 1-diphenylmethyl azetidines

-

, (2008/06/13)

New azetidines, characterized in that they correspond to the general formula (I) STR1 in which R3 represents an amino radical, an alkylamino radical, a dialkylamino radical, a cycloalkylamino radical, an acylamino radical, an alkylacylamino radical, an aminomethyl radical, an alkylaminomethyl radical, an acylaminomethyl radical or an alkylacylaminomethyl radical, in which radicals each acyl fragment may be substituted with one or more halogen, especially fluorine, atoms; and R1, R2, R4, R5 and R6 represent a hydrogen atom or a lower alkyl radical, with the proviso that at least one of them represents a lower alkyl radical, and also their salts.

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