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135412-20-3

4-[2-(diethylamino)ethylsulfanyl]-1,2-dicyano-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 135412-20-3 Structure

  • Basic information

    1. Product Name: 4-[2-(diethylamino)ethylsulfanyl]-1,2-dicyano-benzene
    2. Synonyms: 4-[2-(diethylamino)ethylsulfanyl]-1,2-dicyano-benzene
    3. CAS NO:135412-20-3
    4. Molecular Formula:
    5. Molecular Weight: 259.375
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135412-20-3.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-[2-(diethylamino)ethylsulfanyl]-1,2-dicyano-benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[2-(diethylamino)ethylsulfanyl]-1,2-dicyano-benzene(135412-20-3)
    11. EPA Substance Registry System: 4-[2-(diethylamino)ethylsulfanyl]-1,2-dicyano-benzene(135412-20-3)

  • 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: 135412-20-3(Hazardous Substances Data)

135412-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135412-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,4,1 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 135412-20:
(8*1)+(7*3)+(6*5)+(5*4)+(4*1)+(3*2)+(2*2)+(1*0)=93
93 % 10 = 3
So 135412-20-3 is a valid CAS Registry Number.

135412-20-3Downstream Products

135412-20-3Relevant articles and documents

The synthesis and fluorescence behaviour of new unsymmetrically mono-functionalized carboxy Ge, Ti and Sn phthalocynines

Masilela, Nkosiphile,Nyokong, Tebello

, p. 164 - 169 (2011)

This work reports on the synthesis and fluorescence behaviour of novel unsymmetrically substituted monocarboxy germanium ((OH)2GeMCPc, 3), titanium (OTiMCPc 4) and tin ((ac)2SnMCPc, 5) phthalocyanines. The fluorescence quantum yields

The effects of point of substitution on the electrochemical behavior of new manganese phthalocyanines, tetra-substituted with diethylaminoethanethiol

Akinbulu, Isaac Adebayo,Nyokong, Tebello

, p. 3229 - 3237 (2010)

The syntheses and comparative studies of the spectral, voltammetry and spectroelectrochemical properties of new manganese phthalocyanine complexes, tetra-substituted with diethylaminoethanethio at the peripheral (complex 3a) and non-peripheral positions (

Syntheses and investigation of the effects of position and nature of substituent on the spectral, electrochemical and spectroelectrochemical properties of new cobalt phthalocyanine complexes

Akinbulu, Isaac Adebayo,Nyokong, Tebello

experimental part, p. 1257 - 1270 (2010/04/30)

The syntheses of new cobalt phthalocyanine (CoPc) complexes, tetra-substituted with diethylaminoethanethio at the peripheral (complex 3a) and non-peripheral (complex 3b) positions, and with benzylmercapto at the non-peripheral position (complex 5), are re

Synthesis and evaluation of cationic phthalocyanine derivatives as potential inhibitors of telomerase

Zhang, Lixia,Huang, Jing,Ren, Lige,Bai, Minghui,Wu, Lin,Zhai, Baoping,Zhou, Xiang

, p. 303 - 312 (2008/04/05)

A series of water-soluble cationic phthalocyanine derivatives (1-10) were designed and synthesized to develop novel and potent telomerase inhibitors. These phthalocyanine derivatives as inhibitors of telomerase were investigated via modified telomerase re

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