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459868-73-6

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  • 5-[(2R)-2-Aminopropyl]-2,3-dihydro-1-[3-(phenylmethoxy)propyl]-1H-indole-7-carbonitrile Manufacturer/High quality/Best price/In stock

    Cas No: 459868-73-6

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459868-73-6 Usage

General Description

"(R)-5-(2-aminopropyl)-1-(3-benzyloxypropyl) indoline-7-carbonitrile" is a chemical compound with a structure that includes an indoline ring, a carbonitrile group, and two side chains. The molecule contains an amino group and a benzyl ether group, as well as an asymmetric carbon atom, giving it a chiral property. (R)-5-(2-aminopropyl)-1-(3-benzyloxypropyl) indoline-7-carbonitrile has potential applications in pharmaceutical research and drug development due to its unique structure, which may result in specific biological activities. The synthesis and characterization of this compound have been of interest to chemists and researchers seeking to understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 459868-73-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,9,8,6 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 459868-73:
(8*4)+(7*5)+(6*9)+(5*8)+(4*6)+(3*8)+(2*7)+(1*3)=226
226 % 10 = 6
So 459868-73-6 is a valid CAS Registry Number.

459868-73-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[(2R)-2-aminopropyl]-1-(3-phenylmethoxypropyl)-2,3-dihydroindole-7-carbonitrile

1.2 Other means of identification

Product number -
Other names (R)-5-(2-aminopropyl)-1-(3-benzyloxypropyl)indoline-7-carbonitrile

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:459868-73-6 SDS

459868-73-6Relevant articles and documents

First asymmetric synthesis of Silodosin through catalytic hydrogenation by using Ir-SIPHOX catalysts

Yan, Pu-Cha,Zhang, Xian-Yi,Hu, Xiao-Wei,Zhang, Bin,Zhang, Xiang-Dong,Zhao, Michael,Che, Da-Qing,Li, Yuan-Qiang,Zhou, Qi-Lin

, p. 1449 - 1451 (2013/04/10)

An asymmetric synthesis of Silodosin was accomplished in high yield via catalytic hydrogenation of α,β-unsaturated carboxylic acid derivatives by using chiral catalyst Ir-SIPHOX, followed by Curtius rearrangement. Copyright

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