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1643770-64-2

(S)-1-((S)-3-benzylmorpholino)-2-phenylbutan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1643770-64-2 Structure

  • Basic information

    1. Product Name: (S)-1-((S)-3-benzylmorpholino)-2-phenylbutan-1-one
    2. Synonyms: (S)-1-((S)-3-benzylmorpholino)-2-phenylbutan-1-one
    3. CAS NO:1643770-64-2
    4. Molecular Formula:
    5. Molecular Weight: 323.435
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1643770-64-2.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)-1-((S)-3-benzylmorpholino)-2-phenylbutan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-1-((S)-3-benzylmorpholino)-2-phenylbutan-1-one(1643770-64-2)
    11. EPA Substance Registry System: (S)-1-((S)-3-benzylmorpholino)-2-phenylbutan-1-one(1643770-64-2)

  • 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: 1643770-64-2(Hazardous Substances Data)

1643770-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1643770-64-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,4,3,7,7 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1643770-64:
(9*1)+(8*6)+(7*4)+(6*3)+(5*7)+(4*7)+(3*0)+(2*6)+(1*4)=182
182 % 10 = 2
So 1643770-64-2 is a valid CAS Registry Number.

1643770-64-2Downstream Products

1643770-64-2Relevant articles and documents

Stereoelectronic basis for the kinetic resolution of n-heterocycles with chiral acylating reagents

Hsieh, Sheng-Ying,Wanner, Benedikt,Wheeler, Philip,Beauchemin, Andre M.,Rovis, Tomislav,Bode, Jeffrey W.

supporting information, p. 7228 - 7231 (2014/06/23)

The kinetic resolution of N-heterocycles with chiral acylating agents reveals a previously unrecognized stereoelectronic effect in amine acylation. Combined with a new achiral hydroxamate, this effect makes possible the resolution of various N-heterocycles by using easily prepared reagents. A transition-state model to rationalize the stereochemical outcome of this kinetic resolution is also proposed.

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