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365250-59-5

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365250-59-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 365250-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,5,2,5 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 365250-59:
(8*3)+(7*6)+(6*5)+(5*2)+(4*5)+(3*0)+(2*5)+(1*9)=145
145 % 10 = 5
So 365250-59-5 is a valid CAS Registry Number.

365250-59-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(methoxymethyl)-2,3-dihydro-1H-indole

1.2 Other means of identification

Product number -
Other names 1H-Indole,2,3-dihydro-2-(methoxymethyl)

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:365250-59-5 SDS

365250-59-5Downstream Products

365250-59-5Relevant articles and documents

Cardioselective anti-ischemic ATP-sensitive potassium channel (KATP) openers: Benzopyranyl indoline and indole analogues

Lee, Sunkyung,Yi, Kyu Yang,Kim, Soo-Kyung,Suh, Jeehee,Kim, Nak Jeong,Yoo, Sung-Eun,Lee, Byung Ho,Seo, Ho Won,Kim, Sun-Ok,Lim, Hong

, p. 459 - 471 (2007/10/03)

This paper describes the design, syntheses, and biological evaluations of novel ATP-sensitive potassium channel (KATP) openers, benzopyranyl indoline and indole derivatives. Among those, two enantiomers of indoline-2-carboxylic ethyl esters (14, 18) showed the best cardioprotective activities both in vitro and in vivo, while their vasorelaxation potencies were very low (concentration for 50% inhibition of vasorelaxation >30 μM). The cardioprotective effect of 14 was completely reversed by 5-hydroxydecanoate, a selective mitochondrial KATP blocker, indicating its provable protective mechanism through the mitochondrial KATP opening. In addition, we performed conformational analyses using 2D-NMR, X-ray crystallography and molecular modeling to study the structure-activity relationships in this series of compounds.

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