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2-{[3-cyano-6-phenyl-4-(2-thienyl)-2-pyridinyl]sulfanyl}acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 276671-19-3 Structure
  • Basic information

    1. Product Name: 2-{[3-cyano-6-phenyl-4-(2-thienyl)-2-pyridinyl]sulfanyl}acetamide
    2. Synonyms: 2-{[3-cyano-6-phenyl-4-(2-thienyl)-2-pyridinyl]sulfanyl}acetamide;2-{[3-cyano-6-phenyl-4-(thiophen-2-yl)pyridin-2-yl]sulfanyl}acetamide
    3. CAS NO:276671-19-3
    4. Molecular Formula: C18H13N3OS2
    5. Molecular Weight: 351.45
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 276671-19-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-{[3-cyano-6-phenyl-4-(2-thienyl)-2-pyridinyl]sulfanyl}acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-{[3-cyano-6-phenyl-4-(2-thienyl)-2-pyridinyl]sulfanyl}acetamide(276671-19-3)
    11. EPA Substance Registry System: 2-{[3-cyano-6-phenyl-4-(2-thienyl)-2-pyridinyl]sulfanyl}acetamide(276671-19-3)
  • 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: 276671-19-3(Hazardous Substances Data)

276671-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 276671-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,6,6,7 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 276671-19:
(8*2)+(7*7)+(6*6)+(5*6)+(4*7)+(3*1)+(2*1)+(1*9)=173
173 % 10 = 3
So 276671-19-3 is a valid CAS Registry Number.

276671-19-3Relevant articles and documents

Reactions of styrylthienyl ketone, styryl furyl ketone with thiocyanoacetamide: Synthesis of several new pyridines, thieno[2,3-b]pyridines, pyrido [2′,3′:4,5]thieno[3,2-c]pyridazines and pyrido-[3′,2′:4,5]thieno[3,2-d]pyrimidin one derivatives

Attaby, Fawzy A.

, p. 1 - 12 (2007/10/03)

Styryl thienyl ketone and Styryl furyl ketone 2a,b reacted with thiocyanoacetamide(1) to give the dihydropyridinethiones 3a,b which used as starting material for the synthesis of several heterocyclic compounds. Reaction with several halogeno-esters, halogeno-ketones and chloroacetamide gave 2-S-alkoyl pyridines 5a-d, 10a-d, 13a,b and 19a,b thieno[2,3-c] pyridines 6a,b, 11a,b 14a,b and 20a-d, pyrido[2′,3′,4:5]thieno[2,3-c]pyridazines 8a,b and pyrido[2′.3′:-4,5]thieno[2,3-d]pyrimidinones 15a, b 16a,b and 17a,b. Structures were established based on elemental analyses and spectral data studies.

Cyclizations of Nitriles. LVI. Synthesis and Transformations of Substituted 6-Aryl-3-cyano-4-(2-thienyl)-pyridine-2(1H)-thiones

Sharanin,Matrosova

, p. 1207 - 1211 (2007/10/03)

Sulfurization of 3-aroyl-1,1-dicyano-2-(2-thienyl)propanes afforded substituted 6-aryl-3-cyano-4-(2-thienyl)pyridine-2(1H)-thiones which were alkylated and converted into 3-aminothieno[2,3-b]pyridines.

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