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924663-38-7

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924663-38-7 Usage

Chemical Properties

White Solid

Uses

Different sources of media describe the Uses of 924663-38-7 differently. You can refer to the following data:
1. Rabeprazole N-Oxide (Rabeprazole EP Impurity D) is a Rabeprazole (R070500) impurity.
2. Rabeprazole impurity

Check Digit Verification of cas no

The CAS Registry Mumber 924663-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,4,6,6 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 924663-38:
(8*9)+(7*2)+(6*4)+(5*6)+(4*6)+(3*3)+(2*3)+(1*8)=187
187 % 10 = 7
So 924663-38-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H21N3O4S/c1-13-16(21(22)9-8-17(13)25-11-5-10-24-2)12-26(23)18-19-14-6-3-4-7-15(14)20-18/h3-4,6-9H,5,10-12H2,1-2H3,(H,19,20)

924663-38-7 Well-known Company Product Price

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  • USP

  • (1598031)  Rabeprazole Related Compound B  United States Pharmacopeia (USP) Reference Standard

  • 924663-38-7

  • 1598031-15MG

  • 13,501.80CNY

  • Detail

924663-38-7SDS

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 2-[[4-(3-methoxypropoxy)-3-methyl-1-oxidopyridin-1-ium-2-yl]methylsulfinyl]-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 2-[4-(3-methoxypropoxy)-3-methyl-1-oxypyridin-2-yl-methylsulfinyl]-1H-benzimidazole

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:924663-38-7 SDS

924663-38-7Downstream Products

924663-38-7Relevant articles and documents

Process for the preparation of pyridine-methylsulfinyl compounds

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Page/Page column 6, (2009/04/24)

A process for the preparation of a compound of formula (I), or a salt thereof, wherein Q is ═CR8— or ═N—; and R1-R8 are as herein defined; comprising the reaction of a compound of formula (II), or a salt thereof, wherein Q, R1-R7 are as herein defined; with a reducing agent selected from a trivalent phosphorous compound, an oxidizable solvent and a sulfonic acid chloride; and, if desired, the conversion of a compound of formula (I) to another compound of formula (I) or a salt thereof.

A process for the preparation of pyridine-methylsulfinyl compounds

-

Page/Page column 9, (2008/12/05)

A process for the preparation of a compound of formula (I), or a salt thereof, wherein Q is =CR8- or =N-; and R1-R8 are as herein defined; comprising the reaction of a compound of formula (II), or a salt thereof, wherein Q, R1-R7 are as herein defined; with a reducing agent selected from a trivalent phosphorous compound, an oxidizable solvent and a sulfonic acid chloride; and, if desired, the conversion of a compound of formula (I) to another compound of formula (I) or a salt thereof.

Synthetic studies connected with the preparation of H+/K +-ATPase inhibitors rabeprazole and lansoprazole

Radl, Stanislav,Klecan, Ondrej,Havlicek, Jaroslav

, p. 1447 - 1453 (2007/10/03)

Synthesis of lansoprazole and rabeprazole using common intermediates is devised. The common intermediates, 2-[(4-nitro-3-methylpyridin-2-yl) methanesulfanyl]-1H-benzoimidazole and 2-[(4-chloro-3-methyl-pyridin-2-yl) methanesulfanyl]-1H-benzoimidazole, were prepared in several ways.

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