Cas 1253283-20-3,5-[bis(2,4-dimethoxyphenyl)methyl]-4',5'-bis-methyl-sulfanyl-[2,2']bi{[1,3]dithiolylidene}-4-carbaldehyde

1253283-20-3

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Basic information

Product Name: 5-[bis(2,4-dimethoxyphenyl)methyl]-4',5'-bis-methyl-sulfanyl-[2,2']bi{[1,3]dithiolylidene}-4-carbaldehyde
Synonyms:
CAS NO:1253283-20-3
Molecular Formula:
Molecular Weight: 610.885
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-[bis(2,4-dimethoxyphenyl)methyl]-4',5'-bis-methyl-sulfanyl-[2,2']bi{[1,3]dithiolylidene}-4-carbaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: 5-[bis(2,4-dimethoxyphenyl)methyl]-4',5'-bis-methyl-sulfanyl-[2,2']bi{[1,3]dithiolylidene}-4-carbaldehyde(1253283-20-3)
EPA Substance Registry System: 5-[bis(2,4-dimethoxyphenyl)methyl]-4',5'-bis-methyl-sulfanyl-[2,2']bi{[1,3]dithiolylidene}-4-carbaldehyde(1253283-20-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1253283-20-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1253283-20-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,3,2,8 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1253283-20:
(9*1)+(8*2)+(7*5)+(6*3)+(5*2)+(4*8)+(3*3)+(2*2)+(1*0)=133
133 % 10 = 3
So 1253283-20-3 is a valid CAS Registry Number.

1253283-20-3Upstream product

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1253283-20-3Relevant academic research and scientific papers

Redox-active tetrathiafulvalene and dithiolene compounds derived from allylic 1,4-diol rearrangement products of disubstituted 1,3-dithiole derivatives

Vilela, Filipe,Skabara, Peter J.,Mason, Christopher R.,Westgate, Thomas D. J.,Luquin, Asun,Coles, Simon J.,Hursthouse, Michael B.

, p. 1002 - 1014 (2010)

We present a series of compounds by exploiting the unusual 1,4-aryl shift observed for electron-rich 1,3-dithiole-2-thione and tetrathiafulvalene (TTF) derivatives in the presence of perchloric acid. The mechanistic features of this rearrangement are disc

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