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CAS

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1201183-55-2

(E)-2-nitro-3-m-tolylallyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1201183-55-2 Structure

  • Basic information

    1. Product Name: (E)-2-nitro-3-m-tolylallyl acetate
    2. Synonyms: (E)-2-nitro-3-m-tolylallyl acetate
    3. CAS NO:1201183-55-2
    4. Molecular Formula:
    5. Molecular Weight: 235.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1201183-55-2.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: (E)-2-nitro-3-m-tolylallyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-2-nitro-3-m-tolylallyl acetate(1201183-55-2)
    11. EPA Substance Registry System: (E)-2-nitro-3-m-tolylallyl acetate(1201183-55-2)

  • 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: 1201183-55-2(Hazardous Substances Data)

1201183-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1201183-55-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,1,8 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1201183-55:
(9*1)+(8*2)+(7*0)+(6*1)+(5*1)+(4*8)+(3*3)+(2*5)+(1*5)=92
92 % 10 = 2
So 1201183-55-2 is a valid CAS Registry Number.

1201183-55-2Downstream Products

1201183-55-2Relevant articles and documents

An organocatalytic asymmetric tandem reaction for the construction of bicyclic skeletons

Cao, Chun-Li,Zhou, You-Yun,Zhou, Jian,Sun, Xiu-Li,Tang, Yong,Li, Yu-Xue,Li, Guang-Yu,Sun, Jie

, p. 11384 - 11389 (2009)

Cyclic ketones react with (E)-2-nitroallylic acetates in the presence of catalytic pyrrolidine-thiourea, which affords bicyclic skeletons with four or five stereocenters in one single reaction with up to 98% ee in moderate to high yields. The cooperative

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