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CAS

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1379796-27-6

(RS)-N-benzyl 2-amino-2-(naphthalen-2-yl)acetamide hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1379796-27-6 Structure

  • Basic information

    1. Product Name: (RS)-N-benzyl 2-amino-2-(naphthalen-2-yl)acetamide hydrochloride
    2. Synonyms: (RS)-N-benzyl 2-amino-2-(naphthalen-2-yl)acetamide hydrochloride
    3. CAS NO:1379796-27-6
    4. Molecular Formula:
    5. Molecular Weight: 326.826
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1379796-27-6.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: (RS)-N-benzyl 2-amino-2-(naphthalen-2-yl)acetamide hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: (RS)-N-benzyl 2-amino-2-(naphthalen-2-yl)acetamide hydrochloride(1379796-27-6)
    11. EPA Substance Registry System: (RS)-N-benzyl 2-amino-2-(naphthalen-2-yl)acetamide hydrochloride(1379796-27-6)

  • 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: 1379796-27-6(Hazardous Substances Data)

1379796-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1379796-27-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,7,9 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1379796-27:
(9*1)+(8*3)+(7*7)+(6*9)+(5*7)+(4*9)+(3*6)+(2*2)+(1*7)=236
236 % 10 = 6
So 1379796-27-6 is a valid CAS Registry Number.

1379796-27-6Downstream Products

1379796-27-6Relevant articles and documents

Synthesis, anticonvulsant activity, and neuropathic pain-attenuating activity of N-benzyl 2-amino-2-(hetero)aromatic acetamides

Baruah, Pranjal K.,Dinsmore, Jason,King, Amber M.,Salomé, Christophe,De Ryck, Marc,Kaminski, Rafal,Provins, Laurent,Kohn, Harold

, p. 3551 - 3564 (2012/07/28)

N-Benzyl 2-acetamido-2-substituted acetamides, where the 2-substituent is a (hetero)aromatic moiety, are potent anticonvulsants. We report the synthesis and whole animal pharmacological evaluation of 16 analogues where the terminal 2-acetyl group was removed to give the corresponding primary amino acid derivatives (PAADs). Conversion to the PAAD structure led to a substantial drop in seizure protection in animal tests, demonstrating the importance of the N-acetyl moiety for anticonvulsant activity. However, several of the PAADs displayed notable pain-attenuating activities in a mouse model.

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