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(E)-2-(1,3-benzothiazol-2-yl)-3-(4-fluoroiphenyl)acrylonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • (2E)-2-(1,3-benzothiazol-2-yl)-3-(4-fluorophenyl)prop-2-enenitrile

    Cas No: 1363533-12-3

  • USD $ 1.9-2.9 / Gram

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  • 1363533-12-3 Structure
  • Basic information

    1. Product Name: (E)-2-(1,3-benzothiazol-2-yl)-3-(4-fluoroiphenyl)acrylonitrile
    2. Synonyms: (E)-2-(1,3-benzothiazol-2-yl)-3-(4-fluoroiphenyl)acrylonitrile
    3. CAS NO:1363533-12-3
    4. Molecular Formula:
    5. Molecular Weight: 280.325
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1363533-12-3.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: (E)-2-(1,3-benzothiazol-2-yl)-3-(4-fluoroiphenyl)acrylonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-2-(1,3-benzothiazol-2-yl)-3-(4-fluoroiphenyl)acrylonitrile(1363533-12-3)
    11. EPA Substance Registry System: (E)-2-(1,3-benzothiazol-2-yl)-3-(4-fluoroiphenyl)acrylonitrile(1363533-12-3)
  • 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: 1363533-12-3(Hazardous Substances Data)

1363533-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1363533-12-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,3,5,3 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1363533-12:
(9*1)+(8*3)+(7*6)+(6*3)+(5*5)+(4*3)+(3*3)+(2*1)+(1*2)=143
143 % 10 = 3
So 1363533-12-3 is a valid CAS Registry Number.

1363533-12-3Downstream Products

1363533-12-3Relevant articles and documents

Mycobacterium tuberculosis lysine-?-aminotransferase a potential target in dormancy: Benzothiazole based inhibitors

Reshma, Rudraraju Srilakshmi,Jeankumar, Variam Ullas,Kapoor, Nidhi,Saxena, Shalini,Bobesh, Karyakulam Andrews,Vachaspathy, Astakala Rishi,Kolattukudy, Pappachan E.,Sriram, Dharmarajan

, p. 2761 - 2771 (2017)

MTB lysine-?-aminotransferase (LAT) was found to play a crucial role in persistence and antibiotic tolerance. LAT serves as a potential target in the management of latent tuberculosis. In present work we attempted to derivatize the benzothiazole lead iden

(E)-2-(1,3-Benzothiazol-2-yl)-3-(4-fluorophenyl)acrylonitrile: A chain of π-stacked hydrogen-bonded rings

Trilleras, Jorge,Velásquez, Kelly,Cobo, Justo,Glidewell, Christopher

, p. 671 - 673 (2013)

The title compound, C16H9FN2S, crystallizes as a nonmerohedral twin with twin rotation about the reciprocal-lattice vector [101]*. The molecules are nearly planar and the dihedral angle between the planes of the two aryl r

Microwave-Assisted synthesis under solvent-free conditions of (E)-2-(Benzo[d]thiazol-2-yl)-3-arylacrylonitriles

Trilleras, Jorge E.,Velasquez, Kelly J.,Pacheco, Dency J.,Quiroga, Jairo,Orti?z, Alejandro

experimental part, p. 2396 - 2402 (2012/03/08)

A series of (E)-2-(benzo[d]thiazol-2-yl)-3-arylacrylonitriles was synthesized by microwave assisted Knoevenagel condensation under solvent-free conditions from the corresponding 2-(benzo[d]thiazol-2-yl)acetonitrile and aromatic aldehydes with electrondona

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