Cas 126884-42-2,[5-(3,4-Dichloro-2,5-dioxo-cyclopent-3-enylidene)-7-methyl-8-thioxo-[1,2,4,7]trithiazocan-3-ylidene]-dimethyl-ammonium; chloride

126884-42-2

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Basic information

Product Name: [5-(3,4-Dichloro-2,5-dioxo-cyclopent-3-enylidene)-7-methyl-8-thioxo-[1,2,4,7]trithiazocan-3-ylidene]-dimethyl-ammonium; chloride
Synonyms:
CAS NO:126884-42-2
Molecular Formula:
Molecular Weight: 449.855
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: [5-(3,4-Dichloro-2,5-dioxo-cyclopent-3-enylidene)-7-methyl-8-thioxo-[1,2,4,7]trithiazocan-3-ylidene]-dimethyl-ammonium; chloride(CAS DataBase Reference)
NIST Chemistry Reference: [5-(3,4-Dichloro-2,5-dioxo-cyclopent-3-enylidene)-7-methyl-8-thioxo-[1,2,4,7]trithiazocan-3-ylidene]-dimethyl-ammonium; chloride(126884-42-2)
EPA Substance Registry System: [5-(3,4-Dichloro-2,5-dioxo-cyclopent-3-enylidene)-7-methyl-8-thioxo-[1,2,4,7]trithiazocan-3-ylidene]-dimethyl-ammonium; chloride(126884-42-2)

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
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Hazardous Substances Data: 126884-42-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126884-42-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,8 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126884-42:
(8*1)+(7*2)+(6*6)+(5*8)+(4*8)+(3*4)+(2*4)+(1*2)=152
152 % 10 = 2
So 126884-42-2 is a valid CAS Registry Number.

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126884-42-2Relevant academic research and scientific papers

REACTION OF PERCHLORO-5-METHYLENE-2-CYCLOPENTENE-1,4-DIONE WITH THIOAMIDE NUCLEOPHILES

Talzi, V. P.,Bek, N. O.,Gudoshnikov, S. K.,Safarova, V. I.

, p. 688 - 690 (2007/10/02)

In the reaction of perchloro-5-methylene-2-cyclopentene-1,4-dione with dimethylthioformamide and S-ethyl dimethylthiocarbamate the corresponding salts of the cations of amidothiol ethers are formed as a result of nucleophilic substitution of the two chlorine atoms of the chloromethylene group by two molecules of the thioamide nucleophiles.In the reaction of perchloro-5-methylene-2-cyclopentene-1,4-dione with tetramethylthiuram disulfide the diketone molecule condenses with one thiuram molecule, and hydrogen chloride is eliminated.

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