101387-98-8

• 

• Basic information

  1. Product Name: 2-{[(4-methoxy-3-methylpyridin-2-yl)methyl]sulfinyl}-5,5,7,7-tetramethyl-5,7-dihydroindeno[5,6-d]imidazol-6(1H)-one
  2. Synonyms:
  3. CAS NO:101387-98-8
  4. Molecular Formula: C₂₂H₂₅N₃O₃S
  5. Molecular Weight: 411.5172
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 101387-98-8.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 645.9°C at 760 mmHg
  3. Flash Point: 344.4°C
  4. Appearance: N/A
  5. Density: 1.34g/cm³
  6. Vapor Pressure: 1.43E-16mmHg at 25°C
  7. Refractive Index: 1.665
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 2-{[(4-methoxy-3-methylpyridin-2-yl)methyl]sulfinyl}-5,5,7,7-tetramethyl-5,7-dihydroindeno[5,6-d]imidazol-6(1H)-one(CAS DataBase Reference)
  11. NIST Chemistry Reference: 2-{[(4-methoxy-3-methylpyridin-2-yl)methyl]sulfinyl}-5,5,7,7-tetramethyl-5,7-dihydroindeno[5,6-d]imidazol-6(1H)-one(101387-98-8)
  12. EPA Substance Registry System: 2-{[(4-methoxy-3-methylpyridin-2-yl)methyl]sulfinyl}-5,5,7,7-tetramethyl-5,7-dihydroindeno[5,6-d]imidazol-6(1H)-one(101387-98-8)

• 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: 101387-98-8(Hazardous Substances Data)

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• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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• Indeno[5,6-d]imidazol-6(1H)-one,5,7-dihydro-2-[[(4-methoxy-3-methyl-2-pyridinyl)methyl]sulfinyl]-5,5,7,7-tetramethyl-

  Cas No: 101387-98-8

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• Hangzhou J&H Chemical Co., Ltd.
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101387-98-8 Usage

Chemical class

Sulfoxides and imidazoles

Explanation

Different sources of media describe the Explanation of 101387-98-8 differently. You can refer to the following data:
1. The compound belongs to the class of sulfoxides, which contain a sulfur atom bonded to two different carbon-containing groups, and imidazoles, which are a group of organic compounds containing a five-membered ring with four carbon atoms and one nitrogen atom.
2. The compound has a complex molecular structure, consisting of a combination of pyridine (a six-membered aromatic ring with one nitrogen atom), indene (a fused system of two benzene rings with one common carbon atom), and imidazole moieties.
3. The compound contains a sulfur atom bonded to two different carbon-containing groups, which is characteristic of sulfoxides.
4. The compound is a tetramethylated derivative, meaning it has four methyl groups (CH3) attached to the imidazolone core, which is a five-membered ring system containing four carbon atoms and one nitrogen atom.
5. The structural features of the compound, such as the presence of sulfoxide and imidazole moieties, suggest that it may have potential biological activities, including antioxidant or anti-inflammatory properties.
6. Due to its complex molecular structure and potential biological activities, the compound may have potential applications in the fields of medicinal chemistry and drug development. However, further research is needed to determine its specific biological and pharmacological properties.

Molecular structure

Complex

Sulfoxide

Presence of a sulfur atom bonded to two carbon-containing groups

Tetramethylated derivative

Imidazolone core

Potential biological activities

Antioxidant or anti-inflammatory properties

Potential applications

Medicinal chemistry and drug development

Check Digit Verification of cas no

The CAS Registry Mumber 101387-98-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,3,8 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 101387-98:
(8*1)+(7*0)+(6*1)+(5*3)+(4*8)+(3*7)+(2*9)+(1*8)=108
108 % 10 = 8
So 101387-98-8 is a valid CAS Registry Number.

101387-98-8SDS

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	2-[(4-methoxy-3-methylpyridin-2-yl)methylsulfinyl]-5,5,7,7-tetramethyl-3H-cyclopenta[f]benzimidazol-6-one

1.2 Other means of identification

Product number	-
Other names	Indeno[5,6-d]imidazol-6(1H)-one,5,7-dihydro-2-[[(4-methoxy-3-methyl-2-pyridinyl)methyl]sulfinyl]-5,5,7,7-tetramethyl

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:101387-98-8 SDS

101387-98-8Upstream product

101387-98-8Downstream Products

• 124473-81-0 2-[[(2,4-dichlorobenzyl)dithio]methyl]-4-methoxy-3-methyl-1-(1,5,6,7-tetrahydro-5,5,7,7-tetramethyl-6-oxoindeno-[5,6-d]imidazol-2-yl)pyridinium chloride 
• 124473-89-8 4-methoxy-3-methyl-1-(1,5,6,7-tetrahydro-5,5,7,7-tetramethyl-6-oxoindeno[5,6-d]imidazol-2-yl)-2-[[[m-(trifluoromethyl)phenyl]dithio]methyl]pyridinium chloride 
• 124473-76-3 4-methoxy-3-methyl-2-[(phenethyldithio)methyl]-1-(1,5,6,7-tetrahydro-5,5,7,7-tetramethyl-6-oxoindeno[5,6-d]imidazol-2-yl)pyridinium chloride 
• 124474-24-4 2-[[(2,4-dichlorophenyl)dithio]methyl]-4-methoxy-3-methyl-1-(1,5,6,7-tetrahydro-5,5,7,7-tetramethyl-6-oxoindeno[5,6-d]imidazol-2-yl)pyridinium chloride 
• 124473-31-0 2-[[(2-hydroxyethyl)dithio]methyl]-4-methoxy-3-methyl-1-(1,5,6,7-tetrahydro-5,5,7,7-tetramethyl-6-oxoindeno[5,6-d]imidazol-2-yl)pyridinium chloride 
• 124473-39-8 2-[[(m-chlorophenyl)dithio]methyl]-4-methoxy-3-methyl-1-(1,5,6,7-tetrahydro-5,5,7,7-tetramethyl-6-oxoindeno[5,6-d]imidazol-2-yl)pyridinium chloride 
• 124473-73-0 4-methoxy-3-methyl-1 (1,5,6,7-tetrahydro-5,5,7,7-tetramethyl-6-oxoindeno[5,6-d]imidazol-2-yl)-2-[(o-tolyldithio)methyl]pyridinium chloride 

101387-98-8Relevant articles and documents

METHOD OF USING (H+/K+)ATPASE INHIBITORS AS ANTIVIRAL AGENTS

-

, (2008/06/13)

A class of compounds which are (H+/K+) ATPase inhibitors can be used for the treatment of viral infections. Compounds of particular interest are defined by Formula III: wherein D is N or CH; wherein R7 is one or more radicals selected from hydrido, alkoxy, amino, cyano, nitro, hydroxyl, alkyl, halo, haloalkyl, carboxyl, alkanoyl, nitro, amino, alkylamino, aminocarbonyl , aminosulfonyl , alkylaminocarbonyl, alkylcarbonylamino, alkoxycarbonyl, alkylaminosulfonyl, alkylsulfonylamino, alkylthio, alkyl-sulfinyl and alkylsulfonyl; wherein R8 is selected from hydrido, alkyl and cycloalkyl; wherein R9 is one or more radicals selected from hydrido, alkoxy, amino, alkyl, halo, cyano, nitro, hydroxyl, haloalkyl, nitro, carboxyl, alkanoyl, amino, alkylamino, dialkylamino, aminocarbonyl , alkylaminocarbonyl, alkylcarbonylamino, aminosulfonyl, alkylaminosulfonyl, alkylsulfonylamino, alkoxycarbonyl, alkylthio, alkylsulfinyl and alkylsulfonyl; and wherein R10 and R11 are independently selected from hydrido, alkyl, aryl, alkylcarbonyl and arylcarbonyl wherein the aryl ring may be further substituted with one or more radicals selected from alkyl, halo, hydrazidylcarbonyl, aminocarbonyl and alkoxy; or wherein R10 and R11 together with the nitrogen atom form a heterocyclic ring

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