Welcome to LookChem.com Sign In|Join Free

CAS

  • or

14300-68-6

Post Buying Request

14300-68-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

14300-68-6 Usage

Description

Dimethyl thiophene-2,3-dicarboxylate is a chemical compound that features a thiophene ring with two carboxylate groups and two methyl groups attached to the ring. It is known for its fruity and sweet odor, and its unique chemical structure and properties make it a versatile compound with a range of applications in various industries.

Uses

Used in Pharmaceutical and Agrochemical Industries:
Dimethyl thiophene-2,3-dicarboxylate is utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its chemical structure allows for the creation of a wide range of compounds with potential therapeutic and pesticidal properties.
Used in Fragrance and Flavor Industry:
Due to its distinctive fruity and sweet odor, dimethyl thiophene-2,3-dicarboxylate is employed as a component in the fragrance and flavor industry. It contributes to the development of scents and tastes in a variety of consumer products, such as perfumes, cosmetics, and food items.
Used in Materials Science:
Dimethyl thiophene-2,3-dicarboxylate may have potential applications in materials science due to its unique chemical structure. It could be used in the development of new materials with specific properties, such as conductivity or stability, for various technological applications.
Used in Organic Electronics:
Dimethyl thiophene-2,3-dicarboxylate's properties also make it a candidate for use in the field of organic electronics. It could be incorporated into the design of organic electronic devices, such as organic light-emitting diodes (OLEDs) or organic photovoltaics (OPVs), to enhance their performance or introduce new functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 14300-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,0 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14300-68:
(7*1)+(6*4)+(5*3)+(4*0)+(3*0)+(2*6)+(1*8)=66
66 % 10 = 6
So 14300-68-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H8O4S/c1-11-7(9)5-3-4-13-6(5)8(10)12-2/h3-4H,1-2H3

14300-68-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl Thiophene-2,3-Dicarboxylate

1.2 Other means of identification

Product number -
Other names Dimethyl thiophene-2,3-dicarboxylate

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:14300-68-6 SDS

14300-68-6Relevant articles and documents

SUBSTITUTED PYRIDINES AND PYRIDAZINES WITH ANGIOGENESIS INHIBITING ACTIVITY

-

Page/Page column 36, (2009/03/07)

Substituted pyridines and pyridazines having angiogenesis inhibiting activity and generalized structural formula (I) wherein the ring containing A, B, D, E, and L is phenyl or a nitrogen-containing heterocycle; groups X and Y may be any of a variety of defined linking units; R and R may be defined independent substituents or together may be a ring-defining bridge; ring J may be an aryl, pyridyl, or cycloalkyl group; and G groups may be any of a variety of defined substituents. Pharmaceutical compositions containing these materials, and methods of treating a mammal having a condition characterized by abnormal angiogenesis or hyperpermeability processes using these materials are also disclosed.

Substituted pyridines and pyridazines with angiogenesis inhibiting activity

-

, (2010/02/05)

Substituted pyridazines having angiogenesis inhibiting activity and the generalized structural formula wherein the ring containing A, B, D, E, and L is phenyl or a nitrogen-containing heterocycle; groups X and Y may be any of a variety of defined linking units; R1and R2may be defined independent substituents or together may be a ring-defining bridge; ring J may be an aryl, pyridyl, or cycloalkyl group; and G groups may be any of a variety of defined substituents. Pharmaceutical compositions containing these materials, and methods of treating a mammal having a condition characterized by abnormal angiogenesis or hyperpermiability processes using these materials are also disclosed.

Thermische Cycloadditionen von Acetylendicarbonsaeure-dimethylester an cyclische Enolether und Thioenolether

Gollnick, Klaus,Fries, Siegfried

, p. 848 - 849 (2007/10/02)

-

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 14300-68-6