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CAS

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1207874-02-9

tert-butyl (1S,2S)-(1-(2-fluorophenyl)-2-nitropropyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1207874-02-9 Structure

  • Basic information

    1. Product Name: tert-butyl (1S,2S)-(1-(2-fluorophenyl)-2-nitropropyl)carbamate
    2. Synonyms:
    3. CAS NO:1207874-02-9
    4. Molecular Formula:
    5. Molecular Weight: 298.314
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1207874-02-9.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: tert-butyl (1S,2S)-(1-(2-fluorophenyl)-2-nitropropyl)carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl (1S,2S)-(1-(2-fluorophenyl)-2-nitropropyl)carbamate(1207874-02-9)
    11. EPA Substance Registry System: tert-butyl (1S,2S)-(1-(2-fluorophenyl)-2-nitropropyl)carbamate(1207874-02-9)

  • 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: 1207874-02-9(Hazardous Substances Data)

1207874-02-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1207874-02-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,8,7 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1207874-02:
(9*1)+(8*2)+(7*0)+(6*7)+(5*8)+(4*7)+(3*4)+(2*0)+(1*2)=149
149 % 10 = 9
So 1207874-02-9 is a valid CAS Registry Number.

1207874-02-9Downstream Products

1207874-02-9Relevant articles and documents

Doubly stereocontrolled asymmetric aza-henry reaction with in situ generation of n-boc-imines catalyzed by novel rosin-derived amine thiourea catalysts

Jiang, Xianxing,Zhang, Yifu,Wu, Lipeng,Zhang, Gen,Liu, Xing,Zhang, Hailong,Fu, Dan,Wang, Rui

supporting information; experimental part, p. 2096 - 2100 (2009/12/27)

The doubly stereocontrolled organocatalytic aza-Henry reaction of nitroalkanes to N-Bocimines generated in situ from a variety of substituted α-amido sulfones was investigated for the first time, in general, affording the corresponding products with high

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