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1309476-84-3

t-butyl (E)-3-(2-(3,5-dichlorobenzamido)phenyl)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1309476-84-3 Structure

  • Basic information

    1. Product Name: t-butyl (E)-3-(2-(3,5-dichlorobenzamido)phenyl)acrylate
    2. Synonyms: t-butyl (E)-3-(2-(3,5-dichlorobenzamido)phenyl)acrylate
    3. CAS NO:1309476-84-3
    4. Molecular Formula:
    5. Molecular Weight: 392.282
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1309476-84-3.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: t-butyl (E)-3-(2-(3,5-dichlorobenzamido)phenyl)acrylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: t-butyl (E)-3-(2-(3,5-dichlorobenzamido)phenyl)acrylate(1309476-84-3)
    11. EPA Substance Registry System: t-butyl (E)-3-(2-(3,5-dichlorobenzamido)phenyl)acrylate(1309476-84-3)

  • 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: 1309476-84-3(Hazardous Substances Data)

1309476-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1309476-84-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,4,7 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1309476-84:
(9*1)+(8*3)+(7*0)+(6*9)+(5*4)+(4*7)+(3*6)+(2*8)+(1*4)=173
173 % 10 = 3
So 1309476-84-3 is a valid CAS Registry Number.

1309476-84-3Downstream Products

1309476-84-3Relevant articles and documents

Manipulating micellar environments for enhancing transition metal-catalyzed cross-couplings in water at room temperature

Lipshutz, Bruce H.,Ghorai, Subir,Leong, Wendy Wen Yi,Taft, Benjamin R.,Krogstad, Daniel V.

, p. 5061 - 5073 (2011)

The remarkable effects of added salts on the properties of aqueous micelles derived from the amphiphile PTS are described. Most notably, Heck reactions run in the presence of NaCl lead to couplings on aryl bromides in water at room temperature. Olefin cross- and ring-closing metathesis reactions run in the presence of small amounts of pH-lowering KHSO4 are also accelerated, another phenomenon that does not apply to typical processes in organic media. These salt effects allow, in general, for synthetically valuable C-C bond-forming processes to be conducted under environmentally benign conditions. Recycling of the surfactant is also demonstrated.

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