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CAS

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94225-36-2

Isothiazole, 3-(4-chlorophenyl)-5-[[(1,1-dimethylethyl)dimethylsilyl]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Isothiazole, 3-(4-chlorophenyl)-5-[[(1,1-dimethylethyl)dimethylsilyl]methyl]-

    Cas No: 94225-36-2

  • USD $ 1.9-2.9 / Gram

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  • 94225-36-2 Structure

  • Basic information

    1. Product Name: Isothiazole, 3-(4-chlorophenyl)-5-[[(1,1-dimethylethyl)dimethylsilyl]methyl]-
    2. Synonyms:
    3. CAS NO:94225-36-2
    4. Molecular Formula: C16H22ClNSSi
    5. Molecular Weight: 323.962
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 94225-36-2.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: Isothiazole, 3-(4-chlorophenyl)-5-[[(1,1-dimethylethyl)dimethylsilyl]methyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Isothiazole, 3-(4-chlorophenyl)-5-[[(1,1-dimethylethyl)dimethylsilyl]methyl]-(94225-36-2)
    11. EPA Substance Registry System: Isothiazole, 3-(4-chlorophenyl)-5-[[(1,1-dimethylethyl)dimethylsilyl]methyl]-(94225-36-2)

  • 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: 94225-36-2(Hazardous Substances Data)

94225-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94225-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,2 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 94225-36:
(7*9)+(6*4)+(5*2)+(4*2)+(3*5)+(2*3)+(1*6)=132
132 % 10 = 2
So 94225-36-2 is a valid CAS Registry Number.

94225-36-2Relevant 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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