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4-(2-THIENYLTHIOFORMYL)-MORPHOLINE is a chemical compound with the molecular formula C9H11NOS2. It is a derivative of morpholine, an organic compound that contains a six-membered heterocyclic ring with two oxygen atoms and four carbon atoms. The thiophene ring, a five-membered aromatic ring with one sulfur atom, is attached to the morpholine structure through a thioformyl group (C=S). 4-(2-THIENYLTHIOFORMYL)-MORPHOLINE is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in organic chemistry. Due to its unique structure, it may exhibit specific reactivity and properties that can be exploited in the development of new compounds with desired therapeutic or pesticidal effects.

6391-98-6

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6391-98-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6391-98-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,9 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6391-98:
(6*6)+(5*3)+(4*9)+(3*1)+(2*9)+(1*8)=116
116 % 10 = 6
So 6391-98-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NOS2/c12-9(8-2-1-7-13-8)10-3-5-11-6-4-10/h1-2,7H,3-6H2

6391-98-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name morpholin-4-yl(thiophen-2-yl)methanethione

1.2 Other means of identification

Product number -
Other names HMS1587O15

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:6391-98-6 SDS

6391-98-6Downstream Products

6391-98-6Relevant academic research and scientific papers

Method for promoting elemental sulfur to synthesize thioamide by mixed alkali in water phase

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Paragraph 0053-0056, (2020/07/13)

The invention provides a method for promoting elemental sulfur to synthesize a thioamide compound by a mixed alkali in a water phase, and belongs to the field of organic synthesis. According to the method, an aldehyde compound and an amide compound are us

Mixed bases mediated synthesis of thioamides in water

Li, Jiao,Ren, Xuanhe,Li, Ganzhong,Liang, Helong,Zhao, Yajie,Wang, Zhiwu,Li, Heng,Yuan, Bingxin

, p. 229 - 237 (2020/02/20)

A mixed bases mediated protocol is developed to synthesize thioamides from N-aryl or N-alkylamide, aldehyde and elemental sulfur in water. This reaction requires no addition of external oxidant and avoids large excess of amides. Various functional groups

Rhodamine inhibitors of P-glycoprotein: An amide/thioamide "switch" for ATPase activity

Gannon II, Michael K.,Holt, Jason J.,Bennett, Stephanie M.,Wetzel, Bryan R.,Loo, Tip W.,Bartlett, M. Claire,Clarke, David M.,Sawada, Geri A.,Higgins, J. William,Tombline, Gregory,Raub, Thomas J.,Detty, Michael R.

experimental part, p. 3328 - 3341 (2010/03/26)

We have examined 46 tetramethylrosamine/rhodamine derivatives with structural diversity in the heteroatom of the xanthylium core, the amino substituents of the 3- and 6-positions, and the alkyl, aryl, or heteroaryl group at the 9-substituent. These compou

The Willgerodt-Kindler reaction in water: High chemoselectivity of benzaldehydes over acetophenones

Aghapoor, Kioumars,Mohsenzadeh, Farshid,Khanalizadeh, Golriz,Darabi, Hossein R.

, p. 61 - 65 (2007/10/03)

Water has been found for the first time as a useful solvent in the Willgerodt-Kindler (WK) reaction for the synthesis of benzothiomorpholides in high yield at 80°C for 3 h. This novel approach confronts the WK protocol with a new situation in which water

The reaction of α-amino-substituted diphenylphosphine oxide anions with elemental sulfur and selenium. A new route to thio- and selenoamides

Otten, P. A.,Gen, A. van der

, p. 499 - 506 (2007/10/02)

The lithiated anions of α-amino-substituted diphenylphosphine oxides 1, in which R can be hydrogen, aryl, alkyl and alkenyl, react with two equivalents of sulfur or selenium to form thio- and selenoamides, which can be isolated in good to excellent yields

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