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(4,5-dimethyl-3-thienyl)methanol (SALTDATA: FREE) is a chemical compound characterized by the molecular formula C8H10OS. It is a colorless liquid with a distinctive sweet odor and is utilized in various applications across different industries.

119072-18-3

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119072-18-3 Usage

Uses

Used in Fragrance and Flavor Industry:
(4,5-dimethyl-3-thienyl)methanol (SALTDATA: FREE) is used as a key ingredient in the production of fragrances and flavors due to its strong, sweet scent. It contributes to the creation of various aromas and tastes in consumer products, enhancing their sensory appeal.
Used in Pharmaceutical Industry:
As an intermediate in the synthesis of pharmaceuticals, (4,5-dimethyl-3-thienyl)methanol (SALTDATA: FREE) plays a crucial role in the development of new drugs and medicinal compounds. Its unique chemical structure allows it to be a versatile building block in the formulation of various therapeutic agents.
Used in Organic Compounds Synthesis:
(4,5-dimethyl-3-thienyl)methanol (SALTDATA: FREE) is also employed as an intermediate in the synthesis of other organic compounds. Its reactivity and functional groups make it a valuable component in the production of specialty chemicals and materials.
Safety Precautions:
Given its flammable nature, (4,5-dimethyl-3-thienyl)methanol (SALTDATA: FREE) should be handled with care. It is essential to consult the safety data sheet for proper handling and storage guidelines to ensure the safety of personnel and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 119072-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,0,7 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 119072-18:
(8*1)+(7*1)+(6*9)+(5*0)+(4*7)+(3*2)+(2*1)+(1*8)=113
113 % 10 = 3
So 119072-18-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H10OS/c1-5-6(2)9-4-7(5)3-8/h4,8H,3H2,1-2H3

119072-18-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4,5-dimethylthiophen-3-yl)methanol

1.2 Other means of identification

Product number -
Other names 4.5-Dimethyl-3-thiophenmethanol

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:119072-18-3 SDS

119072-18-3Downstream Products

119072-18-3Relevant academic research and scientific papers

Ethyl 2-Aminothiophene-3-Carboxylates in the Synthesis of Isomeric Thienopyridines

Pokhodylo,Shyyka,Obushak

, p. 1748 - 1755 (2015)

A convenient method for the synthesis of thieno[3,2-c]pyridinones was developed. A number of thiophene derivatives was prepared, and the possibility of using thiophene desamino derivatives for the design of potentially biologically active molecules was demonstrated.

4-OXO-3,4-DIHYDRO-1,2,3-BENZOTRIAZINE MODULATORS OF GPR139

-

Paragraph 0210, (2016/06/13)

The present invention provides a method for treating a disease, disorder or condition associated with GPR139 using compounds of formula 1: which are agonists of GPR139, certain compounds encompassed by formula 1, pharmaceutical compositions thereof, proce

Intramolecular Cycloaddition Reactions with Isobenzofurans, V. - Synthesis of rac-Thiamarmelerin, a Thiophene Analogue of a Naturally Occurring Furanosesquiterpene

Schoening, Axel,Friedrichsen, Willy

, p. 405 - 408 (2007/10/02)

rac-Thiamarmelerin (7b) is prepared by an intramolecular Diels-Alder reaction of a thienofuran. - Keywords: Thienofuran / Cycloadition, intramolecular / Benzthiophene / Marmelerin, thiophene analogue of

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