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119637-67-1

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119637-67-1 Usage

Chemical Properties

White Solid

Uses

Different sources of media describe the Uses of 119637-67-1 differently. You can refer to the following data:
1. antitussive, non-narcotic
2. An antitussive with properties similar to codeine
3. Peripherally acting antitussive.

Check Digit Verification of cas no

The CAS Registry Mumber 119637-67-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,6,3 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 119637-67:
(8*1)+(7*1)+(6*9)+(5*6)+(4*3)+(3*7)+(2*6)+(1*7)=151
151 % 10 = 1
So 119637-67-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H21NO5S/c1-3-21-16(19)10-14(18)17-8-9-23-15(17)11-22-13-7-5-4-6-12(13)20-2/h4-7,15H,3,8-11H2,1-2H3

119637-67-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Moguisteine

1.2 Other means of identification

Product number -
Other names -

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:119637-67-1 SDS

119637-67-1Synthetic route

ethyl potassium malonate
6148-64-7

ethyl potassium malonate

2-(2-methoxy-phenoxymethyl)-1,3-thiazolidine
103181-68-6, 119562-05-9, 119562-07-1

2-(2-methoxy-phenoxymethyl)-1,3-thiazolidine

2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine
119637-67-1

2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine

Conditions
ConditionsYield
Stage #1: ethyl potassium malonate; 2-(2-methoxy-phenoxymethyl)-1,3-thiazolidine With hydrogenchloride; benzotriazol-1-ol In acetone at 0 - 20℃; for 1h;
Stage #2: With dicyclohexyl-carbodiimide In acetone at 0 - 20℃; for 5h; Product distribution / selectivity;
92.27%
Stage #1: ethyl potassium malonate; 2-(2-methoxy-phenoxymethyl)-1,3-thiazolidine With hydrogenchloride In ethyl acetate at 0 - 20℃; for 1h;
Stage #2: With dicyclohexyl-carbodiimide In ethyl acetate at 0 - 20℃; for 6h; Product distribution / selectivity;
90.05%
hydrogen ethyl malonate
1071-46-1

hydrogen ethyl malonate

2-(2-methoxy-phenoxymethyl)-1,3-thiazolidine
103181-68-6, 119562-05-9, 119562-07-1

2-(2-methoxy-phenoxymethyl)-1,3-thiazolidine

2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine
119637-67-1

2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine

Conditions
ConditionsYield
With dicyclohexyl-carbodiimide In ethyl acetate at 0℃; for 6h; Product distribution / selectivity;91.14%
ethyl chlorocarbonylacetate
36239-09-5

ethyl chlorocarbonylacetate

2-(2-methoxy-phenoxymethyl)-1,3-thiazolidine
103181-68-6, 119562-05-9, 119562-07-1

2-(2-methoxy-phenoxymethyl)-1,3-thiazolidine

2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine
119637-67-1

2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine

Conditions
ConditionsYield
With potassium hydrogencarbonate In water; ethyl acetate at 0℃; for 1.5h;85%
2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine
119637-67-1

2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine

methylamine
74-89-5

methylamine

N-methyl 2-<(2-methoxyphenoxy)methyl>-β-oxo-1,3-thiazolidine-3-propanamide

N-methyl 2-<(2-methoxyphenoxy)methyl>-β-oxo-1,3-thiazolidine-3-propanamide

Conditions
ConditionsYield
In ethanol at 40℃; for 20h;92%
2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine
119637-67-1

2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine

ethyl 2-<(2-methoxyphenoxy)methyl>-β-oxo-1,3-thiazolidine-3-propionate 1-oxide

ethyl 2-<(2-methoxyphenoxy)methyl>-β-oxo-1,3-thiazolidine-3-propionate 1-oxide

Conditions
ConditionsYield
With 3-chloro-benzenecarboperoxoic acid In dichloromethane at 0℃; for 2h;84%
2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine
119637-67-1

2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine

2-<(2-methoxyphenoxy)methyl>-β-oxo-1,3-thiazolidine-3-propionic acid
126128-00-5

2-<(2-methoxyphenoxy)methyl>-β-oxo-1,3-thiazolidine-3-propionic acid

Conditions
ConditionsYield
With sodium hydroxide In ethanol for 2h;75%
metabolism in animals and humans after oral administration;
2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine
119637-67-1

2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine

ethyl 2-<(2-methoxyphenoxy)methyl>-β-oxo-1,3-thiazolidine-3-propionate 1,1-dioxide

ethyl 2-<(2-methoxyphenoxy)methyl>-β-oxo-1,3-thiazolidine-3-propionate 1,1-dioxide

Conditions
ConditionsYield
With 3-chloro-benzenecarboperoxoic acid In dichloromethane for 16h; Ambient temperature;70%
N,N-diethylethylenediamine
100-36-7

N,N-diethylethylenediamine

2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine
119637-67-1

2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine

N-(2-Diethylamino-ethyl)-3-[2-(2-methoxy-phenoxymethyl)-thiazolidin-3-yl]-3-oxo-propionamide

N-(2-Diethylamino-ethyl)-3-[2-(2-methoxy-phenoxymethyl)-thiazolidin-3-yl]-3-oxo-propionamide

Conditions
ConditionsYield
In ethanol at 40℃; for 20h;67%
2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine
119637-67-1

2-[2-methoxy-phenoxymethyl)-3-ethoxycarbonylacetyl-1,3-thiazolidine

A

(R,S)-2-(2-methoxy-phenoxymethyl)-3-carboxyacetyl-1,3-thiazolidine, sodium salt

(R,S)-2-(2-methoxy-phenoxymethyl)-3-carboxyacetyl-1,3-thiazolidine, sodium salt

B

2-<(2-methoxyphenoxy)methyl>-β-oxo-1,3-thiazolidine-3-propionic acid
126128-00-5

2-<(2-methoxyphenoxy)methyl>-β-oxo-1,3-thiazolidine-3-propionic acid

Conditions
ConditionsYield
With sodium hydroxide In ethanol
With sodium hydroxide In ethanol

119637-67-1Relevant articles and documents

New process for the synthesis of moguisteine

-

Page/Page column 14-15; 20, (2009/07/10)

The invention relates to a process for the synthesis of moguisteine that is ethyl ester of (R,S)-3-[2-[(2-methoxyphenoxy)methyl]-1,3-thiazolidin-3-yl]-3-oxypropanoic acid which comprises the steps of forming a new cyclic intermediate of formula 2-[(2-methoxyphenoxy)methyl]-1,3-dioxolane (4), forming (R,S)-2-[(2-methoxyphenoxy)methyl]-1,3-thiazolidine (6) and reacting this latter with monoethylmalonic acid (7) or a salt thereof. The moguisteine of the invention is obtained in high yield and purity.

β-carbonyl-carboxyamides of 1,3-thiazolidines

-

, (2008/06/13)

This application relates to compounds of formula I; STR1 wherein R is hydrogen, a linear or branched C1 -C4 -alkyl, allyl or propargyl; X is O, CH2 or S; R1 is --(CH2)n Ra, hydroxy, --O--(CH2)n Ra, --NRbRc or --NH c(CH2)m --NRbRc; Ra is hydrogen, a linear or branched C1 -CH4 -alkyl, phenyl, p-methoxy-phenyl, 3,4,5-trimethoxyphenyl, B-pyryidyl, cyclopentyl or cyclohexyl; Rb and Rc, can be the same or different and are selected independently in the group of hydrogen, linear or branched C1 -C4 -alkyl, cyclohexyl, cyclopentyl, benzyl, hexahydrobenzyl, α,β or γ-pyridylmethyl; or Rb and Rc taken together with the N atom to which they are bound can form a morpholino, piperidino or piperazino residue of formula Rd--N(CH2 --CH2)2 --N-- wherein Rd is hydrogen, linear or branched C1 -C4 -alkyl, benzyl, hexahydrobenzyl, (C6 H5)2 CH--, (p--F--C6 H4)2 CH or B-pyridylmethyl; n is zero or an integer from 1 to 3 and m is 2 or 3; and a process for the preparation thereof.

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