143465-21-8

• 

• Basic information

  1. Product Name: 2-trifluoromethyl-6-hydroxyquinoline
  2. Synonyms:
  3. CAS NO:143465-21-8
  4. Molecular Formula:
  5. Molecular Weight: 213.159
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 143465-21-8.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: 2-trifluoromethyl-6-hydroxyquinoline(CAS DataBase Reference)
  10. NIST Chemistry Reference: 2-trifluoromethyl-6-hydroxyquinoline(143465-21-8)
  11. EPA Substance Registry System: 2-trifluoromethyl-6-hydroxyquinoline(143465-21-8)

• 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: 143465-21-8(Hazardous Substances Data)

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• Downstream Products
• Article

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• 2-(trifluoromethyl)quinolin-6-ol

  Cas No: 143465-21-8

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• 2-trifluoromethyl-6-hydroxyquinoline

  Cas No: 143465-21-8

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• 2-trifluoromethyl-6-hydroxyquinoline

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• 2-(trifluoromethyl)quinolin-6-ol

  Cas No: 143465-21-8

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  Cas No: 143465-21-8

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143465-21-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143465-21-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,4,6 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 143465-21:
(8*1)+(7*4)+(6*3)+(5*4)+(4*6)+(3*5)+(2*2)+(1*1)=118
118 % 10 = 8
So 143465-21-8 is a valid CAS Registry Number.

143465-21-8Upstream product

• 123-30-8 4-amino-phenol 
• 239437-47-9 3,3,4,4,4-Pentafluoro-butyraldehyde 

143465-21-8Downstream Products

143465-21-8Relevant articles and documents

A novel synthesis of 2-fluoroalkyl quinolines

Wang, Quan-Fu,Mao, Yun-Yu,Qin, Chao-Yue,Zhu, Shi-Zheng,Hu, Chang-Ming

, p. 55 - 63 (2000)

2-Fluoroalkyl quinolines are prepared by reacting aniline with α-fluoroalkyl aldehydes or α-fluoroalkyl cyclohexanones in the presence of acetic acid. Under the same reaction condition, 2-aminophenol gives the corresponding 2-fluoroalkyl-8-quinolinols; in some cases, 2-fluoroalkyl benzoxazoles are also formed as minor products.

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