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10177-23-8

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10177-23-8 Usage

General Description

Ethyl 6-(chloromethyl)nicotinate is a chemical compound with the molecular formula C11H12ClNO2. It is a derivative of nicotinic acid, commonly known as niacin, and is classified as an ester. This chemical has a pale yellow color and is commonly used in the pharmaceutical industry as a potential therapeutic agent. It possesses a chloromethyl group which gives it unique properties for potential medicinal applications. Due to its structure and properties, ethyl 6-(chloromethyl)nicotinate has potential pharmacological activities and is being studied for its role in the treatment of various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 10177-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,7 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10177-23:
(7*1)+(6*0)+(5*1)+(4*7)+(3*7)+(2*2)+(1*3)=68
68 % 10 = 8
So 10177-23-8 is a valid CAS Registry Number.

10177-23-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 6-(chloromethyl)pyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names 6-(chloromethyl)-3-pyridinecarboxylic acid ethyl ester

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:10177-23-8 SDS

10177-23-8Relevant articles and documents

A pair of highly biotolerated diamagnetic and paramagnetic iron(II) complexes displaying electroneutrality

Wang,Gondrand,Touti,Hasserodt

, p. 15391 - 15395 (2015)

A pair of structurally analogous macrocyclic iron(ii) complexes with a magnetic off-on relationship is reported that exhibit electroneutrality at neutral pH and high stability in physiological media. This has been achieved by external charge compensation using nicotinate pendent arms. No contact toxicity was observed for cells up to 4 mM for the low-spin and 2 mM for the high-spin complex. These results are a necessary precursor to the future design of turn-on probes with elevated biotolerance.

Towards the synthesis of substituted porphyrins by a pyridyl group bearing a reactive functionality

Ojaimi, Maya El,Habermeyer, Benoit,Gros, Claude P.,Barbe, Jean-Michel

, p. 469 - 480 (2011/03/20)

Pyridyl-substituted porphyrins bearing a reactive functionality were prepared via Suzuki cross-coupling reactions and resulted in very good yields. These compounds are precursors of new porphyrin architectures able to coordinate two metals: one in the porphyrin core and the second around the pyridyl moiety. During the coupling reactions, a higher reactivity of a chloro picolyl group was evidenced compared to a bromo function on the same reacting molecule.

Syntheses and GABA uptake properties of 6-ether- and 6-enol ether-substituted nipecotic acids

N'Goka, Victor,Bissantz, Caterina,Bisel, Philippe,Stenbol, Tine B.,Krogsgaard-Larsen, Povl,Schlewer, Gilbert

, p. 633 - 638 (2007/10/03)

6-Aralkylether- and 6-arylenol-ether-substituted nipecotic acids were synthesized. These analogues are poor GABA uptake inhibitors. The electronegative region concept developed in the N-substituted nipecotic acid series cannot be transferred on the side c

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