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95514-32-2

Benzenemethanamine, 3,5-dichloro-a-[[3-(4-chlorophenyl)-5-isothiazolyl]methylene]-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 95514-32-2 Structure

  • Basic information

    1. Product Name: Benzenemethanamine, 3,5-dichloro-a-[[3-(4-chlorophenyl)-5-isothiazolyl]methylene]-, (Z)-
    2. Synonyms:
    3. CAS NO:95514-32-2
    4. Molecular Formula: C17H11Cl3N2S
    5. Molecular Weight: 381.713
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 95514-32-2.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: Benzenemethanamine, 3,5-dichloro-a-[[3-(4-chlorophenyl)-5-isothiazolyl]methylene]-, (Z)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenemethanamine, 3,5-dichloro-a-[[3-(4-chlorophenyl)-5-isothiazolyl]methylene]-, (Z)-(95514-32-2)
    11. EPA Substance Registry System: Benzenemethanamine, 3,5-dichloro-a-[[3-(4-chlorophenyl)-5-isothiazolyl]methylene]-, (Z)-(95514-32-2)

  • 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: 95514-32-2(Hazardous Substances Data)

95514-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95514-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,5,1 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95514-32:
(7*9)+(6*5)+(5*5)+(4*1)+(3*4)+(2*3)+(1*2)=142
142 % 10 = 2
So 95514-32-2 is a valid CAS Registry Number.

95514-32-2Relevant articles and documents

Ring Transformation Equilibrium (Bond Switch) in the 5-(2-Aminovinyl)isothiazole System via Hypervalent Sulfurane. Synthesis, Structure Determination, and Kinetic Study

Akiba, Kin-ya,Kashiwagi, Kohichi,Ohyama, Yoshihiko,Yamamoto, Yoshuke,Ohkata, Katsuo

, p. 2721 - 2730 (2007/10/02)

Reaction of 3-aryl-5-methylisothiazoles (4) with aromatic nitriles afforded the adducts 3, 5-(2-amino-2-arylvinyl)-3-arylisothiazole derivatives, in the presence of LDA.By employing p-chlorobenzonitrile-15N, the presence of ring transformation from one is

RING-TRANSFORMATION EQUILIBRIUM WITH PARTICIPATION OF ?-BONDED S(IV) IN AN ISOTHIAZOLE SYSTEM. SYNTHESIS OF NON-RING-TRANSFORMED 5-(2-AMINOVINYL)ISOTHIAZOLE DERIVATIVE VIA 1,3-SILYL GROUP SHIFT

Ohkata, Katsuo,Ohyama, Yoshihiko,Watanabe, Yuko,Akiba, Kin-ya

, p. 4561 - 4564 (2007/10/02)

Substituents at 5-position of 5-amino-3-methyl- and 3-p-chlorophenyl-5-methylisothiazoles (7 and 8) were silylated and then lithiated to couple with aromatic nitriles in order to afford the adducts (4 and 5) via 1,3-silyl group shift.Desilylation of 5 wit

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