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70684-82-1

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70684-82-1 Usage

Uses

Methyl 1,2,3,6-Tetrahydropyridine-4-carboxylate Hydrochloride?can be use to synthesize esters of isoguvacine that are potential prodrugs with weak anticonvulsant activities. It is also an intermediate for?1,2,3,6-Tetrahydro-4-pyridinemethanol (T295540) and a methyl ester of?Isoguvacine Hydrochloride (I819560).

Check Digit Verification of cas no

The CAS Registry Mumber 70684-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,8 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70684-82:
(7*7)+(6*0)+(5*6)+(4*8)+(3*4)+(2*8)+(1*2)=141
141 % 10 = 1
So 70684-82-1 is a valid CAS Registry Number.

70684-82-1SDS

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 Methyl 1,2,3,6-tetrahydro-4-pyridinecarboxylate hydrochloride (1: 1)

1.2 Other means of identification

Product number -
Other names methyl 1,2,3,6-tetrhydropyridine-4-carboxylate hydrochloride

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:70684-82-1 SDS

70684-82-1Downstream Products

70684-82-1Relevant articles and documents

Esters of Isoguvacine as Potential Prodrugs

Falch, Erik,Krogsgaard-Larsen, Povl

, p. 285 - 289 (1981)

The syntheses of the methyl ester, butyl ester, (ethoxycarbonyl)methyl ester, and 11 (acyloxy)methyl esters of the potent γ-aminobutyric acid agonist isoguvacine (1,2,3,6-tetrahydropyridine-4-carboxylic acid) are described.The chemical stability of the esters and their in vitro rates of hydrolysis under approximately physiological conditions by nonspecific esterases from human serum were examined.A selected number of the esters were tested for antagonism of convulsions induced by bicuculline, isoniazide, and by electroshock.While the compounds showed only weak activities in the bicuculline and isoniazide tests, a good correlation between in vitro rates of enzymatic hydrolysis and the time of onset of the antagonism of the electroshock-induced convulsions could be found.

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