151983-36-7

• 

• Basic information

  1. Product Name: 5(3H)-Indolizinone,8,8a-dihydro-,(R)-(9CI)
  2. Synonyms: 5(3H)-Indolizinone,8,8a-dihydro-,(R)-(9CI)
  3. CAS NO:151983-36-7
  4. Molecular Formula: C8H9NO
  5. Molecular Weight: 135.16
  6. EINECS: N/A
  7. Product Categories: AMINETERTIARY
  8. Mol File: 151983-36-7.mol
  9. Article Data: 3

• 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: 5(3H)-Indolizinone,8,8a-dihydro-,(R)-(9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: 5(3H)-Indolizinone,8,8a-dihydro-,(R)-(9CI)(151983-36-7)
  11. EPA Substance Registry System: 5(3H)-Indolizinone,8,8a-dihydro-,(R)-(9CI)(151983-36-7)

• 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: 151983-36-7(Hazardous Substances Data)

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• 5(3H)-Indolizinone,8,8a-dihydro-,(R)-(9CI)

  Cas No: 151983-36-7

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151983-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151983-36-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,9,8 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 151983-36:
(8*1)+(7*5)+(6*1)+(5*9)+(4*8)+(3*3)+(2*3)+(1*6)=147
147 % 10 = 7
So 151983-36-7 is a valid CAS Registry Number.

151983-36-7Upstream product

• 1163716-46-8 (S)-1-(2-allyl-2H-pyrrol-1(5H)-yl)prop-2-en-1-one 
• 151983-39-0 3,4-dihydro-1-<(Z)-3-iodo-2-propenyl>-2(1H)-pyridone 

151983-36-7Downstream Products

• 152141-40-7 (S)-hexahydroindolizin-5(1H)-one 
• 18881-13-5 (+)-coniceine 

151983-36-7Relevant articles and documents

Catalytic asymmetric synthesis of a functionalized indolizidine derivative. A useful intermediate suitable for the synthesis of various glycosidase inhibitors

Nukui, Seiji,Sodeoka, Mikiko,Shibasaki, Masakatsu

, p. 4965 - 4968 (1993)

Indolizidine derivative 7 has been sythesized in up 86% ee by an asymmetric Heack reaction (Pd(O)-BPPFOH, Ag-exchanged zeolite) starting with prochiral alkenyl iodide 5. Conversion of 7 to δconiceine (9) is also described.

Asymmetric Heck reaction of alkenyl iodides in the presence of silver salts. Catalytic asymmetric synthesis of decalin and functionalized indolizidine derivatives

Sato,Nukui,Sodeoka,Shibasaki

, p. 371 - 382 (2007/10/02)

Decalin derivatives 3 (up to 80% ee) and indolizidine derivative 6 (up to 86% ee) have been synthesized by an asymmetric Heck reaction starting with prochiral alkenyl iodides 1 and 4, respectively. The important role of silver salts in the asymmetric Heck

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