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(S)-7-(benzyloxymethyl)-2,3-dihydro-1H-pyrrolizin-5(7aH)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1312700-28-9 Structure
  • Basic information

    1. Product Name: (S)-7-(benzyloxymethyl)-2,3-dihydro-1H-pyrrolizin-5(7aH)-one
    2. Synonyms: (S)-7-(benzyloxymethyl)-2,3-dihydro-1H-pyrrolizin-5(7aH)-one
    3. CAS NO:1312700-28-9
    4. Molecular Formula:
    5. Molecular Weight: 243.305
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1312700-28-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-7-(benzyloxymethyl)-2,3-dihydro-1H-pyrrolizin-5(7aH)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-7-(benzyloxymethyl)-2,3-dihydro-1H-pyrrolizin-5(7aH)-one(1312700-28-9)
    11. EPA Substance Registry System: (S)-7-(benzyloxymethyl)-2,3-dihydro-1H-pyrrolizin-5(7aH)-one(1312700-28-9)
  • 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: 1312700-28-9(Hazardous Substances Data)

1312700-28-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1312700-28-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,7,0 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1312700-28:
(9*1)+(8*3)+(7*1)+(6*2)+(5*7)+(4*0)+(3*0)+(2*2)+(1*8)=99
99 % 10 = 9
So 1312700-28-9 is a valid CAS Registry Number.

1312700-28-9Relevant articles and documents

A common approach to pyrrolizidine and indolizidine alkaloids; Formal synthesis of (-)-isoretronecanol, (-)-trachelanthamidine and an approach to the synthesis of (-)-5-epitashiromine and (-)-tashiromine

Reddy, Kotha Kapu Sridhar,Rao, Batchu Venkateswara,Raju, Sagi Satyanarayana

, p. 662 - 668 (2011/07/08)

A common and short stereoselective route is described for the formal synthesis of pyrrolizidine alkaloids, (-)-isoretronecanol and (-)-trachelanthamidine. An approach to the synthesis of indolizidine alkaloids (-)-5-epitashiromine and (-)-tashiromine utilizing ring closing metathesis is also described starting from commercially available and inexpensive l-proline.

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