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methyl 3-chloro-5-phenylthiophene-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1148157-86-1 Structure
  • Basic information

    1. Product Name: methyl 3-chloro-5-phenylthiophene-2-carboxylate
    2. Synonyms: methyl 3-chloro-5-phenylthiophene-2-carboxylate
    3. CAS NO:1148157-86-1
    4. Molecular Formula:
    5. Molecular Weight: 252.721
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1148157-86-1.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: methyl 3-chloro-5-phenylthiophene-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 3-chloro-5-phenylthiophene-2-carboxylate(1148157-86-1)
    11. EPA Substance Registry System: methyl 3-chloro-5-phenylthiophene-2-carboxylate(1148157-86-1)
  • 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: 1148157-86-1(Hazardous Substances Data)

1148157-86-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1148157-86-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,8,1,5 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1148157-86:
(9*1)+(8*1)+(7*4)+(6*8)+(5*1)+(4*5)+(3*7)+(2*8)+(1*6)=161
161 % 10 = 1
So 1148157-86-1 is a valid CAS Registry Number.

1148157-86-1Downstream Products

1148157-86-1Relevant articles and documents

Synthesis of aryl-substituted thieno[3,2-b]thiophene derivatives and their use for N,S-heterotetracene construction

Demina, Nadezhda S.,Kazin, Nikita A.,Rasputin, Nikolay A.,Irgashev, Roman A.,Rusinov, Gennady L.

, p. 2678 - 2683 (2019)

Fiesselmann thiophene synthesis was applied for the convenient construction of thieno[3,2-b]thiophene derivatives. Thus, new 5- or 6-aryl-3-hydroxythieno[3,2-b]thiophene-2-carboxylates were obtained by condensation of 5- or 4-aryl-3-chlorothiophene-2-carb

INHIBITORS OF HISTONE DEACETYLASE

-

Page/Page column 95, (2009/06/27)

ABSTRACT OF THE DISCLOSURE This invention relates to compounds and methods for the inhibition of HDAC enzymatic activity. More particularly, the invention provides for compounds of formula (I), (I) and N-oxides, hydrates, solvates, pharmaceutically acceptable salts, prodrugs and complexes thereof, and racemic and scalemic mixtures, diastereomers and enantiomers thereof, wherein L, M, n, R, W, X and Y are as defined in the specification.

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