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METHYL 4-(4-BROMOPHENYL)THIOPHENE-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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  • 26137-07-5 Structure
  • Basic information

    1. Product Name: METHYL 4-(4-BROMOPHENYL)THIOPHENE-2-CARBOXYLATE
    2. Synonyms: METHYL 4-(4-BROMOPHENYL)THIOPHENE-2-CARBOXYLATE;BUTTPARK 46\15-20;2-THIOPHENECARBOXYLIC ACID, 4-(4-BROMOPHENYL)-, METHYL ESTER
    3. CAS NO:26137-07-5
    4. Molecular Formula: C12H9BrO2S
    5. Molecular Weight: 297.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 26137-07-5.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: METHYL 4-(4-BROMOPHENYL)THIOPHENE-2-CARBOXYLATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: METHYL 4-(4-BROMOPHENYL)THIOPHENE-2-CARBOXYLATE(26137-07-5)
    11. EPA Substance Registry System: METHYL 4-(4-BROMOPHENYL)THIOPHENE-2-CARBOXYLATE(26137-07-5)
  • 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: 26137-07-5(Hazardous Substances Data)

26137-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26137-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,3 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26137-07:
(7*2)+(6*6)+(5*1)+(4*3)+(3*7)+(2*0)+(1*7)=95
95 % 10 = 5
So 26137-07-5 is a valid CAS Registry Number.

26137-07-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-(4-bromophenyl)thiophene-2-carboxylate

1.2 Other means of identification

Product number -
Other names 4-(4-bromo-phenyl)-thiophene-2-carboxylic acid methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:26137-07-5 SDS

26137-07-5Relevant articles and documents

β-Selective C?H Arylation of Electron-Deficient Thiophenes, Pyrroles, and Furans

Liu, Luo-Yan,Qiao, Jennifer X.,Ewing, William R.,Yeung, Kap-Sun,Yu, Jin-Quan

, p. 416 - 418 (2020/02/20)

A general β-C?H arylation of electron-deficient thiophenes, pyrroles, and furans has been developed using ligand-modulated palladium catalyst. The use of a modified norbornene is crucial for reversing the conventional α-selectivity of these substrates. This method features good yields, high β-selectivity, and good tolerance of functional groups.

THIOPHENE AMINO ACID DERIVATIVES, PROCESS FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

-

Page/Page column 30, (2008/06/13)

Compounds of formula (I), in which: R1 and R2, which may be identical or different, independently of each other, each represent a group selected from: hydrogen, halogen, cyano, nitro, halo(C1-C6)alkyl, halo(Csu

5-FLUORO-THIOPEN-COMPOUNDS,THE PROCESS FOR THEIR PREPARATION,THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND THEIR USE AS METALLOPOTENASES INHIBITORS

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Page 21-22, (2008/06/13)

Compounds of formula (I) in which R1 represent a group selected from halo(C1-C6)alkoxy, (C1-C6)alkyl, (C1-C6)alkoxy, (C1-C6)alkylthio, phenyl, cyclohexyl an

The application of vinamidinium salts to the synthesis of 2,4-disubstituted thiophenes

Clemens, Ryan T.,Smith, Stanton Q.

, p. 1319 - 1320 (2007/10/03)

The synthesis of 2,4-disubstituted thiophenes by the condensation of symmetrical vinamidinium salts with methyl thioglycolate has been accomplished for the first time. Simple experimental conditions were used to prepare seven different methyl 4-aryl-2-thi

Novel thiophene derivatives, their process of preparation and the pharmaceutical compositions which comprise them

-

Page/Page column 43, (2010/11/30)

A compound of formula (I) selected from: wherein: X represents oxygen or sulphur, Y represents oxygen, —NH— or —N(C1-C6)alkyl-, Ra represents hydrogen, halogen, (C1-C3)alkyl, hydroxyl or (C1-C3)alkoxy, Rb represents hydrogen, halogen or (C1-C3)alkyl, A represents phenyl, pyridyl, (C5-C6)cycloalkyl or (C5-C6)cycloalkenyl, R1 and R2 each represent a group selected from hydrogen, halogen, cyano, nitro, haloalkyl, haloalkoxy, alkyl, alkenyl, alkynyl, —OR4, —NR4R5, —S(O)nR4, —C(O)R4, —CO2R4, —O—C(O)R4, —C(O)NR4R5, —NR5—C(O)R4, —NR5—SO2R4, -T-CN, -T-OR4, -T-OCF3, -T- NR4R5, -T-S(O)nR4, -T-C(O)R4, -T-CO2R4, -T-O—C(O)R4, -T-C(O)NR4R5, -T-NR4—C(O)R5, -T-NR4—SO2R5, —R6 and -T-R6 in which n, T, R4, R5 and R6 are as defined in the description, R3 represents an —R7 or —U—R11 group in which R7 represents hydrogen, alkyl, aryl, cycloalkyl or heterocycle, U represents a linear or branched alkylene chain and R11 is defined in the description, their optical isomers or their addition salts with a pharmaceutically acceptable acid or base, and their use as inhibitor of metalloproteinase and more specifically of metalloproteinase-12.

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