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CAS

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190383-61-0

1-Piperidinecarboxylic acid, 2-[(2R)-oxiranylmethyl]-, phenylmethyl ester, (2S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 190383-61-0 Structure

  • Basic information

    1. Product Name: 1-Piperidinecarboxylic acid, 2-[(2R)-oxiranylmethyl]-, phenylmethyl ester, (2S)-
    2. Synonyms:
    3. CAS NO:190383-61-0
    4. Molecular Formula: C16H21NO3
    5. Molecular Weight: 275.348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 190383-61-0.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: 1-Piperidinecarboxylic acid, 2-[(2R)-oxiranylmethyl]-, phenylmethyl ester, (2S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Piperidinecarboxylic acid, 2-[(2R)-oxiranylmethyl]-, phenylmethyl ester, (2S)-(190383-61-0)
    11. EPA Substance Registry System: 1-Piperidinecarboxylic acid, 2-[(2R)-oxiranylmethyl]-, phenylmethyl ester, (2S)-(190383-61-0)

  • 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: 190383-61-0(Hazardous Substances Data)

190383-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 190383-61-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,3,8 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 190383-61:
(8*1)+(7*9)+(6*0)+(5*3)+(4*8)+(3*3)+(2*6)+(1*1)=140
140 % 10 = 0
So 190383-61-0 is a valid CAS Registry Number.

190383-61-0Relevant articles and documents

A general entry to 2-(2-hydroxyalkyl)piperidines via iterative asymmetric dihydroxylation to cause enantiomeric enhancement

Takahata, Hiroki,Kubota, Minoru,Momose, Takefumi

, p. 3451 - 3454 (1997)

Both enantiomers of 2-(2-propenyl)piperidine (1) (76-88% ee), prepared via the first AD of 5-hexenyl azide, underwent the second AD to provide all of the four stereoisomeric 2-(2-hydroxypropyl)piperidines (2) with enantiomeric enhancement (>98 ee). An asy

A new synthesis of all four stereoisomers of 2-(2,3- dihydroxypropyl)piperidine via iterative asymmetric dihydroxylation to cause enantiomeric enhancement. Application to asymmetric synthesis of naturally occurring piperidine-related alkaloids

Takahata, Hiroki,Kubota, Minoru,Ikota, Nobuo

, p. 8594 - 8601 (2007/10/03)

Both enantiomers of 2-(2-propenyl)piperidine 1 (76-88% ee), prepared via the first asymmetric dihydroxylation (AD) of 5-hexenyl azide, underwent the second AD to provide all four of the stereoisomeric 2-(2,3- dihydroxypropyl)piperidines 2 with enantiomeric enhancement.(>98% ee). An asymmetric synthesis, starting from 2, of several 2-(2- hydroxyalkyl)piperidine alkaloids [(-)halosaline, (+)-N-methylallosedridine, (+)-8-ethylnorlobelol, (+)-sedridine, (+)-allosedridine, (-)allosedridine, and (+)-N-methylsedridine] and the ant defense alkaloids [(+)-tetraponerine-3 (T-3), T-4, T-7, and T-8] is demonstrated.

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