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14300-68-6

14300-68-6

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14300-68-6 Usage

General Description

Dimethyl thiophene-2,3-dicarboxylate is a chemical compound composed of a thiophene ring with two carboxylate groups and two methyl groups attached to the ring. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Dimethyl thiophene-2,3-dicarboxylate has a fruity and sweet odor, making it suitable for use in the fragrance and flavor industry. It may also have potential applications in materials science and organic electronics due to its unique chemical structure and properties. Overall, dimethyl thiophene-2,3-dicarboxylate is a versatile compound with various industrial and research applications.

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

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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

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Page column 49, (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)

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