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3-(1H-INDOL-6-YL)-ACRYLIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 119160-36-0 Structure
  • Basic information

    1. Product Name: 3-(1H-INDOL-6-YL)-ACRYLIC ACID
    2. Synonyms: RARECHEM AL BK 1265;3-(1H-INDOL-6-YL)-ACRYLIC ACID
    3. CAS NO:119160-36-0
    4. Molecular Formula: C11H9NO2
    5. Molecular Weight: 187.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 119160-36-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-(1H-INDOL-6-YL)-ACRYLIC ACID(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(1H-INDOL-6-YL)-ACRYLIC ACID(119160-36-0)
    11. EPA Substance Registry System: 3-(1H-INDOL-6-YL)-ACRYLIC ACID(119160-36-0)
  • 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: 119160-36-0(Hazardous Substances Data)

119160-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119160-36-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,1,6 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 119160-36:
(8*1)+(7*1)+(6*9)+(5*1)+(4*6)+(3*0)+(2*3)+(1*6)=110
110 % 10 = 0
So 119160-36-0 is a valid CAS Registry Number.

119160-36-0Relevant articles and documents

Heck Diversification of Indole-Based Substrates under Aqueous Conditions: From Indoles to Unprotected Halo-tryptophans and Halo-tryptophans in Natural Product Derivatives

Pubill-Ulldemolins, Cristina,Sharma, Sunil V.,Cartmell, Christopher,Zhao, Jinlian,Cárdenas, Paco,Goss, Rebecca J. M.

, p. 10866 - 10875 (2019)

The blending of synthetic chemistry with biosynthetic processes provides a powerful approach to synthesis. Biosynthetic halogenation and synthetic cross-coupling have great potential to be used together, for small molecule generation, access to natural product analogues and as a tool for chemical biology. However, to enable enhanced generality of this approach, further synthetic tools are needed. Though considerable research has been invested in the diversification of phenylalanine and tyrosine, functionalisation of tryptophans thorough cross-coupling has been largely neglected. Tryptophan is a key residue in many biologically active natural products and peptides; in proteins it is key to fluorescence and dominates protein folding. To this end, we have explored the Heck cross-coupling of halo-indoles and halo-tryptophans in water, showing broad reaction scope. We have demonstrated the ability to use this methodology in the functionalisation of a brominated antibiotic (bromo-pacidamycin), as well as a marine sponge metabolite, barettin.

Aliphatic carboxamides

-

, (2008/06/13)

This invention provides a series of novel heterocyclic aliphatic carboxamides of formula I in which the group >Z--Y--XC=CH--NN--CH=CC=N--NN--N=C and the other radicals have the meanings defined in the following specification. The compounds of formula I are leukotriene antagonists. The invention also provides pharmaceutically acceptable salts of the formula I compounds; pharmaceutical compositions containing the formula I compound, or their salts, for use in the treatment of, for example, allergic or inflammatory diseases, or endotoxic or traumatic shock conditions; and processes for the manufacture of the formula I compounds, as well as intermediates for use in such manufacture.

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