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ethanebis(thioamide), N~1~-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17270-94-9

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17270-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17270-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,7 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17270-94:
(7*1)+(6*7)+(5*2)+(4*7)+(3*0)+(2*9)+(1*4)=109
109 % 10 = 9
So 17270-94-9 is a valid CAS Registry Number.

17270-94-9SDS

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 N-Phenyldithiooxamide

1.2 Other means of identification

Product number -
Other names phenyldithioxoamide

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:17270-94-9 SDS

17270-94-9Relevant academic research and scientific papers

A comparative study of 4-thioxo-(imidazolidines and oxazolidines) and some nucleophilic reagents

Ei-Sharief,Ammar,Mohamed,Ei-Gaby

, p. 215 - 226 (2007/10/03)

The imidazolidines (II) were reacted with amines, H2S and ?-phenylenediamines to give 4-substituted imino derivatives (VI), thiohydantoin (VII) and 1-phenyl-3 -substituted-1H-imidazo[4,5-b]-quinoxaline-2-(3H)-ones(XIII), respectively. Interaction of the oxazolidines (V) with amines, ?-phenylenediamines and ?-aminophenol caused fission of the oxazole ring to produce (XIV, XVII & XIX) respectively.

Convenient synthesis of dithiooxamides from N-arylimino-1,2,3- dithiazoles

Besson, Thierry,Rees, Charles W.,Thiery, Valerie

, p. 1345 - 1348 (2007/10/03)

Among several useful transformations of the readily available N- arylimino-1,2,3-dithiazoles 1 is their rapid conversion by lithium aluminum hydride into the rearranged N-aryldithiooxamides, ArNHCSCSNH2, thus providing a two step synthesis of t

THE REACTION OF NITROACETAMIDES WITH THIONATION REAGENTS SYNTHESIS OF MONO- AND DITHIO- OXALIC ACID DIAMIDES

Harris, Philip A.,Jackson, Arthur,Joule, John A.

, p. 3189 - 3192 (2007/10/02)

Nitroacetamides, R1(R2)N.CO.CH2NO2, react with phosphorus sulphide (P4S10) or 2,4-bis(4-methoxyphenyl)-1,2-dithiadiphosphetane-2,4-disulphide, Lawesson's reagent, to give amidethioamides, R1(R2)N.CO.CS.NH2.

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