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4-(((3-(benzo[d][1,3]dioxol-5-yl)-4-phenylbutyl)amino)-methyl)-N,N-dimethylaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1336873-98-3 Structure
  • Basic information

    1. Product Name: 4-(((3-(benzo[d][1,3]dioxol-5-yl)-4-phenylbutyl)amino)-methyl)-N,N-dimethylaniline
    2. Synonyms: 4-(((3-(benzo[d][1,3]dioxol-5-yl)-4-phenylbutyl)amino)-methyl)-N,N-dimethylaniline
    3. CAS NO:1336873-98-3
    4. Molecular Formula:
    5. Molecular Weight: 402.536
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1336873-98-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(((3-(benzo[d][1,3]dioxol-5-yl)-4-phenylbutyl)amino)-methyl)-N,N-dimethylaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(((3-(benzo[d][1,3]dioxol-5-yl)-4-phenylbutyl)amino)-methyl)-N,N-dimethylaniline(1336873-98-3)
    11. EPA Substance Registry System: 4-(((3-(benzo[d][1,3]dioxol-5-yl)-4-phenylbutyl)amino)-methyl)-N,N-dimethylaniline(1336873-98-3)
  • 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: 1336873-98-3(Hazardous Substances Data)

1336873-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1336873-98-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,6,8,7 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1336873-98:
(9*1)+(8*3)+(7*3)+(6*6)+(5*8)+(4*7)+(3*3)+(2*9)+(1*8)=193
193 % 10 = 3
So 1336873-98-3 is a valid CAS Registry Number.

1336873-98-3Downstream Products

1336873-98-3Relevant articles and documents

Copper and palladium co-catalyzed highly regio-selective 1,2-hydroarylation of terminal 1,3-dienes

Zhang, Rumeng,Li, Qifan,Zhang, Min,Chai, Sida,Duan, Yuqi,Su, Jingfei,Zhao, Qian,Zhang, Chun

, p. 13551 - 13554 (2020/11/17)

A practical copper and palladium co-catalyzed highly regio-selective hydroarylation of terminal 1,3-dienes has been developed. This chemistry afforded the terminal alkenyl group containing products, which are a kind of versatile precursor for organic synthesis, from 1,3-dienes by a practical one-step reaction. With good functional group tolerance, this protocol could be used to make a series of bio-active compounds using readily accessible starting materials. The mechanism of this reaction was explored by control experiments and kinetics studies. This journal is

Compounds and methods for treating cancer by inhibiting the urokinase receptor

-

, (2017/09/15)

Compounds and methods for treating or preventing cancer associated with binding to the urokinase receptor are provided. Biological processes affected by the compounds include cell migration, cell growth, cell adhesion, angiogenesis, cancer cell invasion, apoptosis, tumor formation, tumor progression, metastasis, degradation of the extracellular matrix, pericellular proteolysis, activation of plasminogen, changes in the levels of an extracellular protease, and changes in the levels of a VEGF receptor.

COMPOUNDS AND METHODS FOR TREATING CANCER BY INHIBITING THE UROKINASE RECEPTOR

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, (2013/03/26)

Compounds and methods for treating or preventing cancer associated with binding to the urokinase receptor are provided. Biological processes affected by the compounds include cell migration, cell growth, cell adhesion, angiogenesis, cancer cell invasion, apoptosis, tumor formation, tumor progression, metastasis, degradation of the extracellular matrix, pericellular proteolysis, activation of plasminogen, changes in the levels of an extracellular protease, and changes in the levels of a VEGF receptor.

Virtual screening targeting the urokinase receptor, biochemical and cell-based studies, synthesis, pharmacokinetic characterization, and effect on breast tumor metastasis

Wang, Fang,Li, Jing,Sinn, Anthony L.,Knabe, W. Eric,Khanna, May,Jo, Inha,Silver, Jayne M.,Oh, Kyungsoo,Li, Liwei,Sandusky, George E.,Sledge, George W.,Nakshatri, Harikrishna,Jones, David R.,Pollok, Karen E.,Meroueh, Samy O.

, p. 7193 - 7205 (2012/01/02)

Virtual screening targeting the urokinase receptor (uPAR) led to (±)-3-(benzo[d][1,3]dioxol-5-yl)-N-(benzo[d][1,3]dioxol-5-ylmethyl) -4-phenylbutan-1-amine 1 (IPR-1) and N-(3,5-dimethylphenyl)-1-(4- isopropylphenyl)-5-(piperidin-4-yl)-1H-pyrazole-4-carbox

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