194342-46-6

• 

• Basic information

  1. Product Name: 3-Pyridinemethanol,2,5-dimethyl-(9CI)
  2. Synonyms: 3-Pyridinemethanol,2,5-dimethyl-(9CI)
  3. CAS NO:194342-46-6
  4. Molecular Formula: C₈H₁₁NO
  5. Molecular Weight: 137.17904
  6. EINECS: N/A
  7. Product Categories: PYRIDINE
  8. Mol File: 194342-46-6.mol
  9. Article Data: 1

• 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: 3-Pyridinemethanol,2,5-dimethyl-(9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: 3-Pyridinemethanol,2,5-dimethyl-(9CI)(194342-46-6)
  11. EPA Substance Registry System: 3-Pyridinemethanol,2,5-dimethyl-(9CI)(194342-46-6)

• 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: 194342-46-6(Hazardous Substances Data)

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• 3-PYRIDINEMETHANOL,2,5-DIMETHYL-

  Cas No: 194342-46-6

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194342-46-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194342-46-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,3,4 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 194342-46:
(8*1)+(7*9)+(6*4)+(5*3)+(4*4)+(3*2)+(2*4)+(1*6)=146
146 % 10 = 6
So 194342-46-6 is a valid CAS Registry Number.

194342-46-6Upstream product

• 846541-99-9 6-chloro-2,5-dimethyl-nicotinic acid ethyl ester 
• 57180-01-5 6-hydroxy-2,5-dimethyl-nicotinic acid ethyl ester 
• 31931-53-0 3-(ethoxycarbonyl)-2,5-dimethylpyridine 

194342-46-6Downstream Products

• 1211522-52-9 2,5-dimethyl-3-pyridinecarbaldehyde 
• 695-98-7 2,3,5-trimethyl-pyridine 

194342-46-6Relevant articles and documents

Acetic Acid Promoted Redox Annulations with Dual C-H Functionalization

Zhu, Zhengbo,Seidel, Daniel

supporting information, p. 2841 - 2844 (2017/06/07)

Amines such as 1,2,3,4-tetrahydroisoquinoline undergo redox-neutral annulations with 2-alkylquinoline-3-carbaldehydes as well as the corresponding 4-alkyl isomers and pyridine analogues. These processes involve dual C-H bond functionalization. Acetic acid

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