167111-17-3

• 

• Basic information

  1. Product Name: 1H-Pyrrole,1-(1-oxo-3-butenyl)-(9CI)
  2. Synonyms: 1H-Pyrrole,1-(1-oxo-3-butenyl)-(9CI)
  3. CAS NO:167111-17-3
  4. Molecular Formula: C8H9NO
  5. Molecular Weight: 135.16316
  6. EINECS: N/A
  7. Product Categories: AMINETERTIARY
  8. Mol File: 167111-17-3.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: 1H-Pyrrole,1-(1-oxo-3-butenyl)-(9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: 1H-Pyrrole,1-(1-oxo-3-butenyl)-(9CI)(167111-17-3)
  11. EPA Substance Registry System: 1H-Pyrrole,1-(1-oxo-3-butenyl)-(9CI)(167111-17-3)

• 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: 167111-17-3(Hazardous Substances Data)

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167111-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 167111-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,1,1 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 167111-17:
(8*1)+(7*6)+(6*7)+(5*1)+(4*1)+(3*1)+(2*1)+(1*7)=113
113 % 10 = 3
So 167111-17-3 is a valid CAS Registry Number.

167111-17-3Upstream product

• 54582-33-1 1,1'-carbonyldiimidazole 
• 2622-05-1 allylmagnesium bromide 

167111-17-3Downstream Products

167111-17-3Relevant articles and documents

Conformationally Driven Two- and Three-Photon Cascade Processes in the Stereoselective Photorearrangement of Pyrroles

Koovits, Paul J.,Knowles, Jonathan P.,Booker-Milburn, Kevin I.

, p. 5608 - 5611 (2016)

A TBSO group has been shown to exert a high degree of stereocontrol during the two-photon photocycloaddition/rearrangement of N-butenylpyrroles to complex tricyclic aziridines. Moreover, this and other bulky groups have been shown to change the outcome of the reaction, promoting a new two-photon sequence to tricyclic imines and an unprecedented stereoselective three-photon sequence to azabicyclo[3.3.1]nonanes.

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