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4-Methyl-4,5,6,7-tetrahydrothieno[3,2-c]pyridine is a heterocyclic chemical compound with a molecular formula C8H11NS. It features a unique structure that includes a thieno ring fused with a pyridine ring, making it a valuable building block in the synthesis of pharmaceuticals and agrochemicals. Its versatile properties and potential pharmacological and biological activities, such as anti-cancer and anti-inflammatory effects, contribute to its significance in the development of new drugs and crop protection products.

92503-61-2

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92503-61-2 Usage

Uses

Used in Pharmaceutical Industry:
4-Methyl-4,5,6,7-tetrahydrothieno[3,2-c]pyridine is used as a key intermediate in the synthesis of various pharmaceuticals for its potential as an anti-cancer and anti-inflammatory agent. Its unique structure allows for the development of new drugs with improved therapeutic effects and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical field, 4-Methyl-4,5,6,7-tetrahydrothieno[3,2-c]pyridine serves as a crucial component in the creation of novel crop protection products. Its incorporation into these products can enhance their effectiveness in protecting crops from pests and diseases, thereby contributing to increased agricultural productivity and food security.
Used in Drug Development Research:
4-Methyl-4,5,6,7-tetrahydrothieno[3,2-c]pyridine is utilized in drug development research as a promising scaffold for the design and synthesis of new therapeutic agents. Its structural features and potential biological activities make it an attractive candidate for further exploration and optimization to develop innovative medications for various diseases.
Used in Medicinal Chemistry:
In the realm of medicinal chemistry, 4-Methyl-4,5,6,7-tetrahydrothieno[3,2-c]pyridine is employed as a versatile compound for the exploration of structure-activity relationships and the optimization of drug candidates. Its unique fusion of heterocycles provides a solid foundation for the modification and enhancement of pharmacological properties, leading to the discovery of more effective and safer drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 92503-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,0 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92503-61:
(7*9)+(6*2)+(5*5)+(4*0)+(3*3)+(2*6)+(1*1)=122
122 % 10 = 2
So 92503-61-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NS/c1-6-7-3-5-10-8(7)2-4-9-6/h3,5-6,9H,2,4H2,1H3/p+1/t6-/m0/s1

92503-61-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-4,5,6,7-tetrahydrothieno[3,2-c]pyridine

1.2 Other means of identification

Product number -
Other names HMS1700P14

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:92503-61-2 SDS

92503-61-2Downstream Products

92503-61-2Relevant academic research and scientific papers

An efficient and convenient synthesis of 4,5,6,7-tetrahydrothieno[3,2-c] pyridines by a modified Pictet-Spengler reaction via a formyliminium ion intermediate

Kitabatake, Michikazu,Hashimoto, Aki,Saitoh, Toshiaki,Sano, Takehiro,Mohri, Kunihiko,Horiguchi, Yoshie

experimental part, p. 1903 - 1921 (2011/04/12)

A synthesis of N-formyl-4,5,6,7-tetrahydrothieno[3,2-c]pyridines (5) was achieved in a highly efficient manner via trifluoroacetic acid catalyzed cyclization of formyliminium ion (4), which was produced by imination of 2-(2-thienyl)ethylamine (1) and a carbonyl compound (2) using titanium(IV) tetraisopropoxide followed by formylation with acetic-formic anhydride in a one-pot procedure. This modified Pictet-Spengler reaction provides a convenient method for preparing 4,5,6,7-tetahydrothieno[3,2-c]pyridines (6) possessing various substituents at C-4. The Japan Institute of Heterocyclic Chemistry.

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