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71947-10-9

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71947-10-9 Usage

Purpose

Used to treat high blood pressure and chest pain (angina).

Drug class

Calcium channel blockers.

Mechanism of action

Relaxing and widening blood vessels, making it easier for the heart to pump blood.

Physical properties

White crystalline powder, easily soluble in water.

Administration

Orally in the form of tablets.

Half-life

About 30-50 hours.

Common side effects

Dizziness, swelling of the ankles and feet, and flushing.

Drug interactions

May interact with other medications, so consult a healthcare professional before use.

Check Digit Verification of cas no

The CAS Registry Mumber 71947-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,9,4 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71947-10:
(7*7)+(6*1)+(5*9)+(4*4)+(3*7)+(2*1)+(1*0)=139
139 % 10 = 9
So 71947-10-9 is a valid CAS Registry Number.

71947-10-9SDS

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 1-phenoxy-3-pyrrolidin-1-ylpropan-2-ol

1.2 Other means of identification

Product number -
Other names 1-phenoxy-3-pyrrolidino-propan-2-ol

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:71947-10-9 SDS

71947-10-9Downstream Products

71947-10-9Relevant articles and documents

Highly chemoselective addition of amines to epoxides in water

Azizi, Najmodin,Saidi, Mohammad R.

, p. 3649 - 3651 (2007/10/03)

(Chemical Equation Presented) Aminolysis of a variety of epoxides by aliphatic and aromatic amines in water, in the absence of any catalyst with high yields, is reported. β-Amino alcohols were formed under mild conditions with high selectivity and in excellent yields.

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