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918659-10-6

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918659-10-6 Usage

Uses

Dehydro Azelnidipine is a derivative of Azelnidipine (A808500), a calcium channel blocker that is used as an antihypertensive treatment. Azelnidipine also has anti-atherosclerotic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 918659-10-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,6,5 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 918659-10:
(8*9)+(7*1)+(6*8)+(5*6)+(4*5)+(3*9)+(2*1)+(1*0)=206
206 % 10 = 6
So 918659-10-6 is a valid CAS Registry Number.

918659-10-6SDS

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 azelnidipine

1.2 Other means of identification

Product number -
Other names Dehydro Azelnidipine

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:918659-10-6 SDS

918659-10-6Upstream product

918659-10-6Downstream Products

918659-10-6Relevant articles and documents

Identification and synthesis of impurities formed during preparation of azelnidipine

Rao, K. Sudarshan,Rao, K. Nageswara,Chavan, Bhausaheb,Muralikrishna,Jayashree

, p. 4675 - 4678 (2014/12/10)

Azelnidipine (1), dihydropyridine-based calcium antagonists (DHPs) are one of the widely used drugs for treatment of hypertension. During the laboratory optimization and later during its bulk synthesis the formation of various impurities was observed. The impurities formed were monitored and their structures were tentatively assigned on the basis of their fragmentation patterns in LC-MS. Most of the impurities were synthesized and their assigned constitutions confirmed by co-injection in HPLC. We describe herein the formation, synthesis and characterization of these impurities. Our study will be of immense help to others to obtain chemically high pure azelnidipine.

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