Cas 854278-30-1,dimethyl-selenocarbamic acid <i>Se</i>-[(3-chloro-phenyl)-dimethylcarbamoylselanyl-methyl] ester

854278-30-1

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Basic information

Product Name: dimethyl-selenocarbamic acid Se-[(3-chloro-phenyl)-dimethylcarbamoylselanyl-methyl] ester
Synonyms: dimethyl-selenocarbamic acid Se-[(3-chloro-phenyl)-dimethylcarbamoylselanyl-methyl] ester
CAS NO:854278-30-1
Molecular Formula:
Molecular Weight: 426.663
EINECS: N/A
Product Categories: N/A
Mol File: 854278-30-1.mol
Article Data: 2

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: dimethyl-selenocarbamic acid Se-[(3-chloro-phenyl)-dimethylcarbamoylselanyl-methyl] ester(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl-selenocarbamic acid Se-[(3-chloro-phenyl)-dimethylcarbamoylselanyl-methyl] ester(854278-30-1)
EPA Substance Registry System: dimethyl-selenocarbamic acid Se-[(3-chloro-phenyl)-dimethylcarbamoylselanyl-methyl] ester(854278-30-1)

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: 854278-30-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 854278-30-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,4,2,7 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 854278-30:
(8*8)+(7*5)+(6*4)+(5*2)+(4*7)+(3*8)+(2*3)+(1*0)=191
191 % 10 = 1
So 854278-30-1 is a valid CAS Registry Number.

854278-30-1Upstream product

854278-30-1Downstream Products

854278-30-1Relevant articles and documents

Stannic chloride-induced unsymmetrical C-se bond cleavage of bis(N,N-dimethylcarbamoylseleno)methanes: Novel generation of selenoaldehydes

Gong, Yaling,Shimada, Kazuaki,Nakamura, Hidenori,Fujiyama, Masamichi,Kodama, Akihiro,Otsuki, Miyuki,Matsumoto, Rei,Aoyagi, Shigenobu,Takikawa, Yuji

, p. 125 - 135 (2007/10/03)

Treatment of bis(N,N-dimethylcarbamoylseleno)methanes with SnCl4 afforded β-1,3,5-triselenanes in moderate to high yields, and the key intermediates of the reactions, i.e., acylselonium ions and selenoaldehydes, were successfully trapped by usi

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