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2-[4-(2-carboxyethyl)-5-{5-[3-(2-carboxyethyl)-5-(2-carboxyphenyl)thiophen-2-yl]thiophen-2-yl}thiophen-2-yl]benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1419170-27-6 Structure
  • Basic information

    1. Product Name: 2-[4-(2-carboxyethyl)-5-{5-[3-(2-carboxyethyl)-5-(2-carboxyphenyl)thiophen-2-yl]thiophen-2-yl}thiophen-2-yl]benzoic acid
    2. Synonyms: 2-[4-(2-carboxyethyl)-5-{5-[3-(2-carboxyethyl)-5-(2-carboxyphenyl)thiophen-2-yl]thiophen-2-yl}thiophen-2-yl]benzoic acid
    3. CAS NO:1419170-27-6
    4. Molecular Formula:
    5. Molecular Weight: 632.736
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1419170-27-6.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: 2-[4-(2-carboxyethyl)-5-{5-[3-(2-carboxyethyl)-5-(2-carboxyphenyl)thiophen-2-yl]thiophen-2-yl}thiophen-2-yl]benzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[4-(2-carboxyethyl)-5-{5-[3-(2-carboxyethyl)-5-(2-carboxyphenyl)thiophen-2-yl]thiophen-2-yl}thiophen-2-yl]benzoic acid(1419170-27-6)
    11. EPA Substance Registry System: 2-[4-(2-carboxyethyl)-5-{5-[3-(2-carboxyethyl)-5-(2-carboxyphenyl)thiophen-2-yl]thiophen-2-yl}thiophen-2-yl]benzoic acid(1419170-27-6)
  • 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: 1419170-27-6(Hazardous Substances Data)

1419170-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1419170-27-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,9,1,7 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1419170-27:
(9*1)+(8*4)+(7*1)+(6*9)+(5*1)+(4*7)+(3*0)+(2*2)+(1*7)=146
146 % 10 = 6
So 1419170-27-6 is a valid CAS Registry Number.

1419170-27-6Downstream Products

1419170-27-6Relevant articles and documents

NOVEL COMPOUNDS AND THEIR USE IN THERAPY

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Page/Page column 91; 92, (2013/03/26)

The present invention relates to novel chemical compounds formula (I) (C)n-B-(A)m-B-(C)n (I) wherein m is 0 or 1, and n is independently 0, 1, 2 or 3, A, each B and each C are independently selected from phenylene and five-and six-membered heteroaromatic rings, and for a terminal ring B or C also from bicyclic heteroaromatic fused rings having seven to ten ring members, wherein the bond between at least two of the rings A to C may be replaced by a carbonyl group (-CO-), wherein at least two of the rings A to C are substituted with one or two groups R, and wherein each ring A to C further optionally is substituted with one or two groups R1. The compounds are useful in therapy, especially therapy of a mammal suffering from a disease involving misfolded or aggregated forms of proteins.

NOVEL THIOPHENE COMPOUNDS AND METHOD FOR IN VIVO IMAGING

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Page/Page column 96-97, (2013/03/26)

The present invention relates to novel labelled compounds of formula (I) (C)n-B-(A)m-B-(C)n (I) wherein m is 0 or 1, and n is independently 0, 1, 2 or 3, A, each B and each C are independently selected from phenylene and five- and six-membered heteroaromatic rings, and for a terminal ring B or C also from bicyclic heteroaromatic fused rings having seven to ten ring members, wherein the bond between at least two of the rings A to C may be replaced by a carbonyl group ( -CO- ), wherein at least two of the rings A to C are substituted with one or two groups R, and wherein each ring A to C further optionally is substituted with one or two groups R1, for use in imaging amyloid deposits and aggregated protein in living patients. The invention further relates to imaging methods using labelled or unlabelled compounds of formual I and the use of unlabelled compounds in such methods.

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