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63285-84-7

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63285-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63285-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,8 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63285-84:
(7*6)+(6*3)+(5*2)+(4*8)+(3*5)+(2*8)+(1*4)=137
137 % 10 = 7
So 63285-84-7 is a valid CAS Registry Number.

63285-84-7 Well-known Company Product Price

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  • Alfa Aesar

  • (B25288)  3-Phenoxythiophene, 97%   

  • 63285-84-7

  • 1g

  • 576.0CNY

  • Detail
  • Alfa Aesar

  • (B25288)  3-Phenoxythiophene, 97%   

  • 63285-84-7

  • 5g

  • 2611.0CNY

  • Detail
  • Alfa Aesar

  • (B25288)  3-Phenoxythiophene, 97%   

  • 63285-84-7

  • 25g

  • 10483.0CNY

  • Detail

63285-84-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-PHENOXYTHIOPHENE

1.2 Other means of identification

Product number -
Other names 3-Thienylphenylether

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:63285-84-7 SDS

63285-84-7Relevant articles and documents

Biphenylsulfonamides and derivatives thereof that modulate the activity of endothelin

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, (2008/06/13)

Biphenylsulfonamides and methods for modulating or altering the activity of the endothelin family of peptides are provided. In particular, bicyclic or tricyclic carbon or heterocyclic ring biphenylsulfonamides and methods using these sulfonamides for inhibiting the binding of an endothelin peptide to an endothelin receptor by contacting the receptor with the sulfonamide are provided. Methods for treating endothelin-mediated disorders by administering effective amounts of one or more of these sulfonamides or prodrugs thereof that inhibit or increase the activity of endothelin are also provided.

THIENYL-, FURYL- AND PYRROLYL- SULFONAMIDES AND DERIVATIVES THEREOF THAT MODULATE THE ACTIVITY OF ENDOTHELIN

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, (2008/06/13)

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SULFONAMIDES AND DERIVATIVES THEREOF THAT MODULATE THE ACTIVITY OF ENDOTHELIN

-

, (2008/06/13)

Sulfonamides and methods using these sulfonamides for inhibiting the binding of an endothelin peptide to an endothelin receptor by contacting the receptor with the sulfonamide are provided. Methods for treating endothelin-mediated disorders by administering effective amounts of one or more of these sulfonamides or prodrugs thereof that inhibit or increase the activity of endothelin are also provided. The sulfonamides have formula I: STR1 in which Ar 1 is a 3-or 5-isoxazolyl and Ar. sup.2 is selected from among alkyl, including straight and branched chains, aromatic rings, fused aromatic rings and heterocyclic rings, including 5-membered heterocycles with one, two or more heteroatoms and fused ring analogs thereof and 6-membered rings with one, two or more heteroatoms and fused ring analogs thereof. Ar 2 is preferably thiophenyl, furyl, pyrrolyl, naphthyl, and phenyl. Compounds in which Ar. sup.1 is a 4-halo-substituted isoxazole are more active than the corresponding alkyl-substituted compound and compounds in which Ar 1 is substituted at this position with a higher alkyl tend to exhibit greater affinity for ET B receptors than the corresponding lower alkyl-substituted compound.

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