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ClC4H3NCC6H5C4N(CH3)2CH2CH3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1355953-56-8 Structure
  • Basic information

    1. Product Name: ClC4H3NCC6H5C4N(CH3)2CH2CH3
    2. Synonyms: ClC4H3NCC6H5C4N(CH3)2CH2CH3
    3. CAS NO:1355953-56-8
    4. Molecular Formula:
    5. Molecular Weight: 310.826
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1355953-56-8.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: ClC4H3NCC6H5C4N(CH3)2CH2CH3(CAS DataBase Reference)
    10. NIST Chemistry Reference: ClC4H3NCC6H5C4N(CH3)2CH2CH3(1355953-56-8)
    11. EPA Substance Registry System: ClC4H3NCC6H5C4N(CH3)2CH2CH3(1355953-56-8)
  • 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: 1355953-56-8(Hazardous Substances Data)

1355953-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1355953-56-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,5,9,5 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1355953-56:
(9*1)+(8*3)+(7*5)+(6*5)+(5*9)+(4*5)+(3*3)+(2*5)+(1*6)=188
188 % 10 = 8
So 1355953-56-8 is a valid CAS Registry Number.

1355953-56-8Relevant articles and documents

Rational design of fluorescent probes for targeted: In vivo nitroreductase visualization

Chen, Ji-An,Gao, Jie,Gu, Xianfeng,Li, Mimi,Tan, Jiahui,Yin, Xiaofan,Zhao, Zhen

, p. 4744 - 4747 (2020)

Nitroreductase (NTR) has been recognized as a biomarker for identifying the hypoxic status of cancers. Therefore, it is of high scientific interest to design effective fluorescent probes for tracking NTR activity. However, studies on elucidation of the structure-performance relationship of fluorescent probes and those providing valuable insight into optimized probe design have rarely been reported. Three BODIPY based fluorescent probes were made by conjugation of para-, ortho-, and meta-nitrobenzene to the BODIPY core via a thiolether bond, respectively. Our study revealed that the linkage and nitro substituent position significantly influence the capability of nitroreductase detection.

Design, synthesis and photophysical studies of BODIPY-o, m, p-phenylenediamine-based probes: Insights into their responsiveness under different pH conditions

Jin, Guofan,Li, Binxian,Xiao, Fuyan,Zhao, Wantao

, (2021)

In this paper, a series of novel phenylenediamine-fluoroboron pyrrole fluorescent derivatives were prepared which have distinct responsiveness under different hydrogen ion concentration (pH) conditions. It is noticed that the products showed excellent flu

BODIPY-based sulfoxide: Synthesis, photophysical characterization and response to benzenethiols

Zhao, Chunchang,Wang, Xuzhe,Cao, Jian,Feng, Peng,Zhang, Jinxin,Zhang, Yanfen,Yang, Yang,Yang, Zhenjun

, p. 328 - 332 (2013/02/22)

Two BODIPY dyes bearing a sulfur containing function at the 3-position are reported. The 3-benzylthio compound shows spectroscopic features of the classical BODIPY platform, showing minor solvent dependent spectral shift, a relative small Stokes shift and

Development of a borondipyrromethene-based Zn2+ fluorescent probe: Solvent effects on modulation sensing ability

Zhao, Chunchang,Zhang, Yulin,Feng, Peng,Cao, Jian

experimental part, p. 831 - 838 (2012/03/07)

A borondipyrromethene-based Zn2+ fluorescent probe BODPAQ was designed and synthesized. The chelators in BODPAQ, 2,2′-dipicolylamine (DPA) and 8-aminoquinoline (AQ), coordinate to Zn2+ in a synergic manner. As a result, BODPAQ displa

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