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CAS

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297173-62-7

1-[2'-N,N-di(phenylmethyl)amino]ethanoyl-3,4(S)-dimethyl-5(R)-phenylimidazolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 297173-62-7 Structure

  • Basic information

    1. Product Name: 1-[2'-N,N-di(phenylmethyl)amino]ethanoyl-3,4(S)-dimethyl-5(R)-phenylimidazolidin-2-one
    2. Synonyms: 1-[2'-N,N-di(phenylmethyl)amino]ethanoyl-3,4(S)-dimethyl-5(R)-phenylimidazolidin-2-one
    3. CAS NO:297173-62-7
    4. Molecular Formula:
    5. Molecular Weight: 427.546
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 297173-62-7.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-[2'-N,N-di(phenylmethyl)amino]ethanoyl-3,4(S)-dimethyl-5(R)-phenylimidazolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[2'-N,N-di(phenylmethyl)amino]ethanoyl-3,4(S)-dimethyl-5(R)-phenylimidazolidin-2-one(297173-62-7)
    11. EPA Substance Registry System: 1-[2'-N,N-di(phenylmethyl)amino]ethanoyl-3,4(S)-dimethyl-5(R)-phenylimidazolidin-2-one(297173-62-7)

  • 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: 297173-62-7(Hazardous Substances Data)

297173-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 297173-62-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,7,1,7 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 297173-62:
(8*2)+(7*9)+(6*7)+(5*1)+(4*7)+(3*3)+(2*6)+(1*2)=177
177 % 10 = 7
So 297173-62-7 is a valid CAS Registry Number.

297173-62-7Relevant articles and documents

syn-Selective boron mediated aldol condensations for the asymmetric synthesis of β-hydroxy-α-amino acids

Caddick,Parr,Pritchard

, p. 5963 - 5966 (2000)

Imidazolidinone-bound glycine enolate derivatives have been shown to undergo aldol condensation with aromatic and aliphatic aldehydes in good yields and with excellent stereocontrol (62-84%, 93-95% d.e.). Removal of the pendant imidazolidinone auxiliary and hydrogenolysis affords the β-hydroxy- α-amino acid derivatives. (C) 2000 Elsevier Science Ltd.

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