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1449411-42-0

(3R,4R)-1-benzyl-4-(4-bromophenyl)-2-oxopiperidine-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1449411-42-0 Structure

  • Basic information

    1. Product Name: (3R,4R)-1-benzyl-4-(4-bromophenyl)-2-oxopiperidine-3-carbonitrile
    2. Synonyms:
    3. CAS NO:1449411-42-0
    4. Molecular Formula:
    5. Molecular Weight: 369.261
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1449411-42-0.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: (3R,4R)-1-benzyl-4-(4-bromophenyl)-2-oxopiperidine-3-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R,4R)-1-benzyl-4-(4-bromophenyl)-2-oxopiperidine-3-carbonitrile(1449411-42-0)
    11. EPA Substance Registry System: (3R,4R)-1-benzyl-4-(4-bromophenyl)-2-oxopiperidine-3-carbonitrile(1449411-42-0)

  • 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: 1449411-42-0(Hazardous Substances Data)

1449411-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1449411-42-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,4,1 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1449411-42:
(9*1)+(8*4)+(7*4)+(6*9)+(5*4)+(4*1)+(3*1)+(2*4)+(1*2)=160
160 % 10 = 0
So 1449411-42-0 is a valid CAS Registry Number.

1449411-42-0Upstream product

1449411-42-0Downstream Products

1449411-42-0Relevant articles and documents

One-pot synthesis of optically enriched 2-piperidinones from aliphatic aldehydes and cyanoacrylamides

He, Ying,Kang, Tai-Ran,Liu, Quan-Zhong,Chen, Lian-Mei,Tu, Yi-Lian,Liu, Ya-Jun,Chen, Tang-Bin,Wang, Zhi-Qiang,Liu, Jie,Xie, Yong-Mei,Yang, Jin-Liang,He, Long

, p. 4054 - 4057 (2013)

A highly stereoselective one-pot reaction of aliphatic aldehydes and cyanoacrylamides has been developed. The one-pot reaction includes an organocatalytic Michael addition followed by an intramolecular hemiaminalization. After reduction, optically enriched 2-piperidinones with three contiguous chiral centers were obtained in up to 95% yield and 9:1 dr with 99% ee.

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