399044-23-6

• 

• Basic information

  1. Product Name: 5(1H)-Indolizinone,2,3,8,8a-tetrahydro-,(8aS)-(9CI)
  2. Synonyms: 5(1H)-Indolizinone,2,3,8,8a-tetrahydro-,(8aS)-(9CI);(8aS)-2,3,8,8a-tetrahydro-5(1H)-Indolizinone
  3. CAS NO:399044-23-6
  4. Molecular Formula: C8H11NO
  5. Molecular Weight: 137.18
  6. EINECS: N/A
  7. Product Categories: AMINETERTIARY
  8. Mol File: 399044-23-6.mol
  9. Article Data: 2

• 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(1H)-Indolizinone,2,3,8,8a-tetrahydro-,(8aS)-(9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: 5(1H)-Indolizinone,2,3,8,8a-tetrahydro-,(8aS)-(9CI)(399044-23-6)
  11. EPA Substance Registry System: 5(1H)-Indolizinone,2,3,8,8a-tetrahydro-,(8aS)-(9CI)(399044-23-6)

• 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: 399044-23-6(Hazardous Substances Data)

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399044-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 399044-23-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,9,0,4 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 399044-23:
(8*3)+(7*9)+(6*9)+(5*0)+(4*4)+(3*4)+(2*2)+(1*3)=176
176 % 10 = 6
So 399044-23-6 is a valid CAS Registry Number.

399044-23-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	(8aS)-2,3,8,8a-tetrahydro-1H-indolizin-5-one

1.2 Other means of identification

Product number	-
Other names	5(1h)-indolizinone,2,3,8,8a-tetrahydro-,(8as)

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:399044-23-6 SDS

399044-23-6Upstream product

• 115393-77-6 tert-butyl (S)-2-vinylpyrrolidine-1-carboxylate 
• 399044-21-4 N-[(1,1-dimethylethoxy)carbonyl]-2-(2-propen-1-yl)pyrrolidine 
• 338945-22-5 (S)-2-iodomethyl-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 23356-96-9 (S)-1-Pyrrolidin-2-yl-methanol 
• 132959-53-6 (2S)-2-(2-propenyl)pyrrolidine 
• 69610-40-8 N-(tert-butoxycarbonyl)-L-prolinol 
• 399044-22-5 (2S)-1-acryloyl-2-(2-propenyl)pyrrolidine 

399044-23-6Downstream Products

399044-23-6Relevant articles and documents

A convenient entry to indolizidine alkaloids using Kharasch type reactions

Morales-Chamorro, Maricela,Meza-González, Jorge,Cordero-Vargas, Alejandro

supporting information, p. 4892 - 4894 (2015/07/28)

A convenient entry to indolizidine alkaloids based on a free-radical atom transfer reaction (ATRA or Kharasch reaction) as the key step is reported. The strategy is based on the free radical reaction between ethyl iodoacetate and an l-proline derivative serving as a radical acceptor. The key intermediate obtained after the radical reaction is used for the synthesis of indolizidine (-)-167B and of an advanced intermediate for the synthesis of (+)-dendroprimine.

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