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Nepaprazole is a benzimidazole derivative that has been found to be more potent than Omeprazole in terms of proton pump inhibition and antisecretory activity. It is a pharmaceutical compound with potential applications in the treatment of various gastrointestinal disorders.

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  • 156601-79-5 Structure
  • Basic information

    1. Product Name: Nepaprazole
    2. Synonyms: Nepaprazole
    3. CAS NO:156601-79-5
    4. Molecular Formula: C18H19N3O2S
    5. Molecular Weight: 341.433
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156601-79-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 626.4°Cat760mmHg
    3. Flash Point: 332.6°C
    4. Appearance: /
    5. Density: 1.39g/cm3
    6. Vapor Pressure: 1.32E-15mmHg at 25°C
    7. Refractive Index: 1.702
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Nepaprazole(CAS DataBase Reference)
    11. NIST Chemistry Reference: Nepaprazole(156601-79-5)
    12. EPA Substance Registry System: Nepaprazole(156601-79-5)
  • 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: 156601-79-5(Hazardous Substances Data)

156601-79-5 Usage

Uses

Used in Pharmaceutical Industry:
Nepaprazole is used as a proton pump inhibitor for its potent ability to inhibit gastric acid secretion. This makes it a valuable treatment option for conditions such as gastroesophageal reflux disease (GERD), peptic ulcers, and other acid-related disorders. Its enhanced potency compared to Omeprazole suggests that it may offer improved efficacy and faster relief for patients suffering from these conditions.
Additionally, Nepaprazole's antisecretory activity indicates its potential use in reducing the secretion of various substances in the body, which could have further applications in treating a range of medical conditions beyond gastrointestinal disorders. However, more research would be needed to explore these potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 156601-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,6,0 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 156601-79:
(8*1)+(7*5)+(6*6)+(5*6)+(4*0)+(3*1)+(2*7)+(1*9)=135
135 % 10 = 5
So 156601-79-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H19N3O2S/c1-23-15-10-11-19-17-12(15)6-2-5-9-16(17)24(22)18-20-13-7-3-4-8-14(13)21-18/h3-4,7-8,10-11,16H,2,5-6,9H2,1H3,(H,20,21)/t16-,24+/m1/s1

156601-79-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(1H-benzimidazol-2-ylsulfinyl)-4-methoxy-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridine

1.2 Other means of identification

Product number -
Other names UNII-UZT71BQ5OO

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:156601-79-5 SDS

156601-79-5Downstream Products

156601-79-5Relevant articles and documents

Syntheses and antiulcer activities of novel 2-[(6,7,8,9-tetrahydro-5H- cyclohepta[b]pyridin-9-yl)sulfinyl]-1H-benzimidazole analogues

Yamada,Goto,Shimanuki,Narita

, p. 718 - 720 (1994)

A synthetic study on a series of benzimidazole derivatives including cycloalka[b]pyridine moiety has been carried out. Among these compounds synthesized, novel antipeptic agent with 6,7,8,9-tetrahydro-5H- cyclohepta[b]pyridin moiety (TY-11345) was found to be superior to omeprazole in (H++K+)-ATPase inhibitory activity and antisecretory potencies.

Synthetic study of 2-[(6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-9-yl)-sulfinyl]-1H-benzimidazole analogs and their biological broperties as novel proton pump inhibitors

Yamada,Goto,Yamaguchi,Aihara,Kogi,Narita

, p. 421 - 431 (1995)

A series of 2-[(cycloalka[b]pyridinyl)sulfinyl]-1H-benzimidazoles (11) was synthesized and tested for antisecretory activity against pentagastrin-induced gastric acid secretion in rats. A novel benzimidazole derivative containing a cyclohepta[b]pyridine m

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