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4-BROMO-2-ETHYNYL-THIOPHENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 690266-87-6 Structure
  • Basic information

    1. Product Name: 4-BROMO-2-ETHYNYL-THIOPHENE
    2. Synonyms: 4-BROMO-2-ETHYNYL-THIOPHENE
    3. CAS NO:690266-87-6
    4. Molecular Formula: C6H3BrS
    5. Molecular Weight: 187.05702
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 690266-87-6.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: 4-BROMO-2-ETHYNYL-THIOPHENE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-BROMO-2-ETHYNYL-THIOPHENE(690266-87-6)
    11. EPA Substance Registry System: 4-BROMO-2-ETHYNYL-THIOPHENE(690266-87-6)
  • 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: 690266-87-6(Hazardous Substances Data)

690266-87-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 690266-87-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,0,2,6 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 690266-87:
(8*6)+(7*9)+(6*0)+(5*2)+(4*6)+(3*6)+(2*8)+(1*7)=186
186 % 10 = 6
So 690266-87-6 is a valid CAS Registry Number.

690266-87-6Relevant articles and documents

Bis(het)aryl-1,2,3-triazole quinuclidines as α7 nicotinic acetylcholine receptor ligands: Synthesis, structure affinity relationships, agonism activity, [18F]-radiolabeling and PET study in rats

Ouach, Aziz,Vercouillie, Johnny,Bertrand, Emilie,Rodrigues, Nuno,Pin, Frederic,Serriere, Sophie,Boiaryna, Liliana,Chartier, Agnes,Percina, Nathalie,Tangpong, Pakorn,Gulhan, Zuhal,Mothes, Celine,Deloye, Jean-Bernard,Guilloteau, Denis,Page, Guylene,Suzenet, Franck,Buron, Frederic,Chalon, Sylvie,Routier, Sylvain

, p. 449 - 469 (2019/07/03)

In this paper we describe the design and synthesis of bis(Het)Aryl-1,2,3-triazole quinuclidine α7R ligands using an efficient three-step sequence including a Suzuki-Miyaura cross coupling reaction with commercially available and home-made boron derivatives. The exploration of SAR required the preparation of uncommon boron derivatives. Forty final drugs were tested for their ability to bind the target and nine of them exhibited Ki values below nanomolar concentrations. The best scores were always obtained when the 5-phenyl-2-thiophenyl core was attached to the triazole. The selectivity of these compounds towards the nicotinic α4β2 and serotoninergic 5HT3 receptors was assessed and their brain penetration was quantified by the preparation and in vivo evaluation of two [18F] radiolabelled derivatives. It can be expected from our results that some of these compounds will be suitable for further developments and will have effects on cognitive disorders.

Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds

-

, (2008/06/13)

The present invention relates to alkyne compounds of general formula I wherein the groups and residues A, B, W, X, Y, Z, R1 and R2 have the meanings given in claim 1. The invention further relates to pharmaceutical compositions containing at least one alkyne according to the invention. In view of their MCH-receptor antagonistic activity the pharmaceutical compositions according to the invention are suitable for the treatment of metabolic disorders and/or eating disorders, particularly obesity, bulimia, anorexia, hyperphagia and diabetes.

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