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CAS

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1607483-36-2

(E)-methyl 4-(6-bromohexyloxy)cinnamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1607483-36-2 Structure

  • Basic information

    1. Product Name: (E)-methyl 4-(6-bromohexyloxy)cinnamate
    2. Synonyms: (E)-methyl 4-(6-bromohexyloxy)cinnamate
    3. CAS NO:1607483-36-2
    4. Molecular Formula:
    5. Molecular Weight: 341.245
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1607483-36-2.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)-methyl 4-(6-bromohexyloxy)cinnamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-methyl 4-(6-bromohexyloxy)cinnamate(1607483-36-2)
    11. EPA Substance Registry System: (E)-methyl 4-(6-bromohexyloxy)cinnamate(1607483-36-2)

  • 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: 1607483-36-2(Hazardous Substances Data)

1607483-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1607483-36-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,7,4,8 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1607483-36:
(9*1)+(8*6)+(7*0)+(6*7)+(5*4)+(4*8)+(3*3)+(2*3)+(1*6)=172
172 % 10 = 2
So 1607483-36-2 is a valid CAS Registry Number.

1607483-36-2Relevant articles and documents

Design and synthesis of photoactive ionic liquids

Avo, Joao,Cunha-Silva, Luis,Lima, Joao Carlos,Jorge Parola

, p. 2582 - 2585 (2014)

Two ionic liquids with photoisomerizable p-hydroxycinnamic acid moieties were synthesized and characterized by X-ray crystallography and DSC, and their photochemistry was studied in solution and neat conditions. Irradiation at absorption maxima led to trans-cis photoisomerization and resulted in significant reduction of melting temperatures of the ionic liquids. X-ray structures of both compounds show an intricate network of supramolecular interactions before irradiation. Physical and chemical transformations are completely reversible upon irradiation at lower wavelengths of ionic liquid solutions in acetonitrile.

Synthesis, in?vitro inhibitory activity, kinetic study and molecular docking of novel N-alkyl–deoxynojirimycin derivatives as potential α-glucosidase inhibitors

Lin, Ping,Zeng, Jia-Cheng,Chen, Ji-Guang,Nie, Xu-Liang,Yuan, En,Wang, Xiao-Qiang,Peng, Da-Yong,Yin, Zhong-Ping

, p. 1879 - 1890 (2020/10/06)

A series of novel N-alkyl-1-deoxynojirimycin derivatives 25 ～ 44 were synthesised and evaluated for their in?vitro α-glucosidase inhibitory activity to develop α-glucosidase inhibitors with high activity. All twenty compounds exhibited α-glucosidase inhib

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