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328974-80-7

5-ETHENYL-L-PROLINE METHYL ESTER HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 328974-80-7 Structure

  • Basic information

    1. Product Name: 5-ETHENYL-L-PROLINE METHYL ESTER HYDROCHLORIDE
    2. Synonyms: H-L-PRO(5S-VINYL)-OME HCL;5-ETHENYL-L-PROLINE METHYL ESTER HYDROCHLORIDE;L-Proline, 5-ethenyl-, methyl ester, (5S)- (9CI);Methyl (2S,5S)-5-vinyl-2-pyrrolidinecarboxylate hydrochloride;5-Ethenyl-L-Pro methyl ester
    3. CAS NO:328974-80-7
    4. Molecular Formula: C8H14ClNO2
    5. Molecular Weight: 191.66
    6. EINECS: N/A
    7. Product Categories: GLYCINESCAFFOLD;PYRROLE;CARBOXYLICESTER
    8. Mol File: 328974-80-7.mol

  • 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-ETHENYL-L-PROLINE METHYL ESTER HYDROCHLORIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-ETHENYL-L-PROLINE METHYL ESTER HYDROCHLORIDE(328974-80-7)
    11. EPA Substance Registry System: 5-ETHENYL-L-PROLINE METHYL ESTER HYDROCHLORIDE(328974-80-7)

  • 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: 328974-80-7(Hazardous Substances Data)

328974-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 328974-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,9,7 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 328974-80:
(8*3)+(7*2)+(6*8)+(5*9)+(4*7)+(3*4)+(2*8)+(1*0)=187
187 % 10 = 7
So 328974-80-7 is a valid CAS Registry Number.

328974-80-7Downstream Products

328974-80-7Relevant articles and documents

A sequential electrochemical oxidation - Olefin metathesis strategy for the construction of bicyclic lactam based peptidomimetics

Beal, Laura M.,Moeller, Kevin D.

, p. 4639 - 4642 (1998)

A sequential electrochemical amide oxidation - ring closing olefin metathesis sequence has been used to overcome problems associated with the synthesis of seven-membered ring lactam containing bicyclic peptidomimetics. The synthesis of several previously unavailable bicyelic lactam building blocks for constructing constrained thyroliberin analogs is described.

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