173936-20-4

• 

• Basic information

  1. Product Name: 1-Azabicyclo[2.2.1]heptan-3-one,oxime,[1R-(Z)]-(9CI)
  2. Synonyms: 1-Azabicyclo[2.2.1]heptan-3-one,oxime,[1R-(Z)]-(9CI)
  3. CAS NO:173936-20-4
  4. Molecular Formula: C6H10N2O
  5. Molecular Weight: 126.16
  6. EINECS: N/A
  7. Product Categories: AMINETERTIARY
  8. Mol File: 173936-20-4.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: 1-Azabicyclo[2.2.1]heptan-3-one,oxime,[1R-(Z)]-(9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: 1-Azabicyclo[2.2.1]heptan-3-one,oxime,[1R-(Z)]-(9CI)(173936-20-4)
  11. EPA Substance Registry System: 1-Azabicyclo[2.2.1]heptan-3-one,oxime,[1R-(Z)]-(9CI)(173936-20-4)

• 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: 173936-20-4(Hazardous Substances Data)

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173936-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173936-20-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,9,3 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 173936-20:
(8*1)+(7*7)+(6*3)+(5*9)+(4*3)+(3*6)+(2*2)+(1*0)=154
154 % 10 = 4
So 173936-20-4 is a valid CAS Registry Number.

173936-20-4Upstream product

• 142034-96-6 Z-(R)-(-)-1-Azabicyclo[2.2.1]heptan-3-one 
• 21472-89-9 1-azabicyclo[2.2.1]heptan-3-one 

173936-20-4Downstream Products

173936-20-4Relevant articles and documents

PREPARATION OF STEREOCHEMICALLY PURE OXIMES WITH MUSCARINIC ACTIVITY

-

, (2008/06/13)

The instant invention is a selective formation of the Z-oxime and O-alkylation of 1-azabicyclo[2.2.1]heptan-3-one and 1-azabicyclo[2.2. 2] heptan-3-one oximes to produce compounds with muscarinic activity. The process is capable of scale-up for industrial purposes as it provides better yields and ease of preparation. Intermediates are also described.

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