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100442-33-9

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  • 2,N-Dimethyl-N-(3,3-diphenylpropyl)-1-amino-2-propanol CAS:100442-33-9 Chinese manufacturers high-quality

    Cas No: 100442-33-9

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100442-33-9 Usage

Chemical Properties

Slightly Brown Liquid

Uses

Different sources of media describe the Uses of 100442-33-9 differently. You can refer to the following data:
1. Lercanidipine Intermediate
2. Lercanidipine Intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 100442-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,4 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100442-33:
(8*1)+(7*0)+(6*0)+(5*4)+(4*4)+(3*2)+(2*3)+(1*3)=59
59 % 10 = 9
So 100442-33-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H27NO/c1-20(2,22)16-21(3)15-14-19(17-10-6-4-7-11-17)18-12-8-5-9-13-18/h4-13,19,22H,14-16H2,1-3H3

100442-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,N-Dimethyl-N-(3,3-Diphenylpropyl)-1-Amino-2-Propanol

1.2 Other means of identification

Product number -
Other names 1-(3,3-Diphenyl-N-methylpropylamino)-2-methyl-2-propanol

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:100442-33-9 SDS

100442-33-9Relevant articles and documents

Asymmetric N-(3,3-diphenylpropyl)aminoalkyl esters of 4-aryl-2,6- dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acids with antihypertensive activity

Leonardi, Amedeo,Motta, Gianni,Pennini, Renzo,Testa, Rodolfo,Sironi, Giorgio,Catto, Alberto,Cerri, Alberto,Zappa, Marco,Bianchi, Giorgio,Nardi, Dante

, p. 399 - 420 (2007/10/03)

A series of asymmetric 4-aryl-1,4-dihydropyridine-3,5-dicarboxylates characterized by the presence of a 3,3-diphenylpropylamino moiety in one of the ester groups were synthesized. They exhibited remarkable antihypertensive activity in spontaneously hypertensive rats as well as affinity for the 1,4- dihydropyridines binding site labelled by 3H-nitrendipine in the calcium channel. Introduction of this bulky and lipophilic amine confers to the whole series an elevated level of antihypertensive activity and a long duration of action, a structure-dependent modulation of the activity being found only in the subset characterized by the presence of a branched propylene bridge between the ester and the amino groups. The presence of the amino group is essential for oral activity. Out of this series, compound 9u (Rec 15/2375- lercanidipine) was selected for clinical development and obtained marketing authorization as an antihypertensive in several countries.

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