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3-Amino-4,5,6-trimethylthieno[2,3-b]pyridine-2-carboxamide is a complex organic compound with the molecular formula C11H14N4OS. It features a thieno[2,3-b]pyridine core, which is a fused ring system consisting of a thiophene and a pyridine. The molecule has three methyl groups attached to the thiophene ring, contributing to its lipophilic nature. The 3-amino group and the 2-carboxamide group provide the molecule with basic and amide functionalities, respectively. 3-Amino-4,5,6-trimethylthieno[2,3-b]pyridine-2-carboxamide is of interest in medicinal chemistry due to its potential as a precursor or building block for the synthesis of various pharmaceuticals and agrochemicals. Its specific applications may vary, but the compound's unique structure suggests it could be involved in the development of new drugs targeting specific receptors or enzymes.

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  • 119003-37-1 Structure
  • Basic information

    1. Product Name: 3-Amino-4,5,6-trimethylthieno[2,3-b]pyridine-2-carboxamide
    2. Synonyms: 3-Amino-4,5,6-trimethylthieno[2,3-b]pyridine-2-carboxamide;3-amino-4,5,6-trimethylthieno[2,3-b]pyridine-2-carboxamide(SALTDATA: FREE)
    3. CAS NO:119003-37-1
    4. Molecular Formula: C11H13N3OS
    5. Molecular Weight: 235.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 119003-37-1.mol
  • Chemical Properties

    1. Melting Point: 264-266 °C
    2. Boiling Point: 462°C at 760 mmHg
    3. Flash Point: 233.2°C
    4. Appearance: /
    5. Density: 1.336g/cm3
    6. Vapor Pressure: 1.03E-08mmHg at 25°C
    7. Refractive Index: 1.702
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 16.10±0.30(Predicted)
    11. CAS DataBase Reference: 3-Amino-4,5,6-trimethylthieno[2,3-b]pyridine-2-carboxamide(CAS DataBase Reference)
    12. NIST Chemistry Reference: 3-Amino-4,5,6-trimethylthieno[2,3-b]pyridine-2-carboxamide(119003-37-1)
    13. EPA Substance Registry System: 3-Amino-4,5,6-trimethylthieno[2,3-b]pyridine-2-carboxamide(119003-37-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 119003-37-1(Hazardous Substances Data)

119003-37-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119003-37-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,0,0 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 119003-37:
(8*1)+(7*1)+(6*9)+(5*0)+(4*0)+(3*3)+(2*3)+(1*7)=91
91 % 10 = 1
So 119003-37-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H13N3OS/c1-4-5(2)7-8(12)9(10(13)15)16-11(7)14-6(4)3/h12H2,1-3H3,(H2,13,15)

119003-37-1SDS

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 3-amino-4,5,6-trimethylthieno[2,3-b]pyridine-2-carboxamide

1.2 Other means of identification

Product number -
Other names 3-Amino-4,5,6-trimethyl-thieno<2,3-b>pyridin-2-carbonsaeureamid

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:119003-37-1 SDS

119003-37-1Downstream Products

119003-37-1Relevant articles and documents

New version of multicomponent condensation leading to 3-amino-2-acyl-4,5,6-trimethylthieno[2,3-b]pyridines

Dyachenko

, p. 1578 - 1583 (2015/12/30)

3-Amino-2-acyl-4,5,6-trimethylthieno[2,3-b]pyridines were synthesized by multicomponent condensation of acetaldehyde, cyanothioacetamide, 4-(but-2-en-2-yl)-morpholine, and a-haloketones.

Synthesis and evaluation of pyrido-thieno-pyrimidines as potent and selective Cdc7 kinase inhibitors

Zhao, Chunlin,Tovar, Christian,Yin, Xuefeng,Xu, Qui,Todorov, Ivan T.,Vassilev, Lyubomir T.,Chen, Li

scheme or table, p. 319 - 323 (2011/02/26)

Cdc7 kinase plays a critical role in the regulation of DNA replication in eukaryotic cells and has been proposed as a target for cancer therapy. We have identified a class of Cdc7/Dbf4 inhibitors with a pyrido-thieno-pyrimidine core structure. Synthesis o

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