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SDZ-201 106 (+/-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97730-95-5

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97730-95-5 Usage

Uses

SDZ-201106 (+/-), (DPI-201106) is a positive inotropic and calcium sensitizing agent.

Check Digit Verification of cas no

The CAS Registry Mumber 97730-95-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,7,3 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97730-95:
(7*9)+(6*7)+(5*7)+(4*3)+(3*0)+(2*9)+(1*5)=175
175 % 10 = 5
So 97730-95-5 is a valid CAS Registry Number.
InChI:InChI=1/C29H30N4O2/c30-19-24-18-26-27(31-24)12-7-13-28(26)35-21-25(34)20-32-14-16-33(17-15-32)29(22-8-3-1-4-9-22)23-10-5-2-6-11-23/h1-13,18,25,29,31,34H,14-17,20-21H2

97730-95-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[3-(4-benzhydrylpiperazin-1-yl)-2-hydroxypropoxy]-1H-indole-2-carbonitrile

1.2 Other means of identification

Product number -
Other names Dpi 201-106

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:97730-95-5 SDS

97730-95-5Downstream Products

97730-95-5Relevant academic research and scientific papers

An efficient synthesis of 4-hydroxy-1H-indole-2-carbonitrile and its conversion to DPI 201-106

Estep

, p. 507 - 514 (2007/10/02)

A three-step synthesis of 4-hydroxy-1H-indole-2-carbonitrile (3) from commercially available 1,5,6,7-tetrahydro-4H-indol-4-one (4) via cyanation and subsequent halogenation/dehydrohalogenation proceeds in 84% overall yield. The conversion of 3 into positive inotrope DPI 201-106 (1) is also described.

3-Aminopropoxyaryl derivatives, their preparation and pharmaceutical compositions containing them

-

, (2008/06/13)

The compounds of formula I STR1 where R 1, R 2 and R have various significances, and physiologically acceptable hydrolyzable derivatives thereof having the hydroxy group in the 2 position of the 3-aminopropoxy side chain in esterified form, are useful as

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