13896-81-6

• 

• Basic information

  1. Product Name: 1-(quinolin-2-ylsulfanyl)propan-2-one
  2. Synonyms: 1-(Quinolin-2-ylsulfanyl)acetone; 2-propanone, 1-(2-quinolinylthio)-
  3. CAS NO:13896-81-6
  4. Molecular Formula: C₁₂H₁₁NOS
  5. Molecular Weight: 217.2868
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 13896-81-6.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 371°C at 760 mmHg
  3. Flash Point: 178.2°C
  4. Appearance: N/A
  5. Density: 1.22g/cm³
  6. Vapor Pressure: 1.06E-05mmHg at 25°C
  7. Refractive Index: 1.642
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 1-(quinolin-2-ylsulfanyl)propan-2-one(CAS DataBase Reference)
  11. NIST Chemistry Reference: 1-(quinolin-2-ylsulfanyl)propan-2-one(13896-81-6)
  12. EPA Substance Registry System: 1-(quinolin-2-ylsulfanyl)propan-2-one(13896-81-6)

• 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: 13896-81-6(Hazardous Substances Data)

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• SDS
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• Downstream Products
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• 2-Propanone,1-(2-quinolinylthio)-

  Cas No: 13896-81-6

• USD $ 3.0-3.0 / Kilogram

• 1 Kilogram

• 1-100 Metric Ton/Month

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• 2-Propanone,1-(2-quinolinylthio)- cas 13896-81-6

  Cas No: 13896-81-6

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13896-81-6 Usage

Structure

A derivative of quinoline with a sulfanyl group attached to the second carbon of a propan-2-one chain

Functional groups

Quinoline, sulfanyl, and propan-2-one

Applications

a. Chemical reactions and organic synthesis
b. Formation of heterocyclic compounds

Pharmacological properties

a. Potential anti-inflammatory agent
b. Potential antioxidant agent

Material development

Shown promise in the development of new materials

Synthesis

Used as a building block for the synthesis of complex organic molecules

Check Digit Verification of cas no

The CAS Registry Mumber 13896-81-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,9 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13896-81:
(7*1)+(6*3)+(5*8)+(4*9)+(3*6)+(2*8)+(1*1)=136
136 % 10 = 6
So 13896-81-6 is a valid CAS Registry Number.

13896-81-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-quinolin-2-ylsulfanylpropan-2-one

1.2 Other means of identification

Product number	-
Other names	2-Propanone,1-(2-quinolinylthio)

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13896-81-6 SDS

13896-81-6Upstream product

• 2637-37-8 Quinoline-2-thiol 
• 78-95-5 chloroacetone 

13896-81-6Downstream Products

13896-81-6Relevant articles and documents

Electrolytic partial fluorination of organic compounds. 31.1 Regioselective anodic fluorination of 2-quinolyl and 4-(7- trifluoromethyl)quinolyl sulfides and the factors affecting its optimization

Dawood, Kamal M.,Fuchigami, Toshio

, p. 138 - 143 (1999)

Electrochemical fluorination of 2-quinolyl and 4-(7- trifluoromethyl)quinolyl sulfides bearing an electron-withdrawing group at the position α to the sulfur atom was studied. Fluorination was successfully carried out using Et4NF·nHF (n = 3, 4) and Et3N·3HF as a supporting electrolyte and a fluoride ion source in dimethoxyethane in a divided cell to provide the corresponding α-fluorinated sulfides in good yields. A trifluoromethyl group positioned on the quinoline ring significantly enhanced anodic α-fluorination. 4-(Methylthio)-7-(trifluoromethyl)quinoline was also found to undergo anodic fluorination efficiently. Solvent effects of various donor numbers were also established.

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