Cas 1370229-72-3,dithiocarbonic acid S-{1-((tert-butoxycarbonylamino)methyl)-4-[methanesulfonyl(3,5-dimethoxyphenyl)amino]-4-oxo-butyl} ester O-ethyl ester

1370229-72-3

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Basic information

Product Name: dithiocarbonic acid S-{1-((tert-butoxycarbonylamino)methyl)-4-[methanesulfonyl(3,5-dimethoxyphenyl)amino]-4-oxo-butyl} ester O-ethyl ester
Synonyms: dithiocarbonic acid S-{1-((tert-butoxycarbonylamino)methyl)-4-[methanesulfonyl(3,5-dimethoxyphenyl)amino]-4-oxo-butyl} ester O-ethyl ester
CAS NO:1370229-72-3
Molecular Formula:
Molecular Weight: 550.719
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: dithiocarbonic acid S-{1-((tert-butoxycarbonylamino)methyl)-4-[methanesulfonyl(3,5-dimethoxyphenyl)amino]-4-oxo-butyl} ester O-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: dithiocarbonic acid S-{1-((tert-butoxycarbonylamino)methyl)-4-[methanesulfonyl(3,5-dimethoxyphenyl)amino]-4-oxo-butyl} ester O-ethyl ester(1370229-72-3)
EPA Substance Registry System: dithiocarbonic acid S-{1-((tert-butoxycarbonylamino)methyl)-4-[methanesulfonyl(3,5-dimethoxyphenyl)amino]-4-oxo-butyl} ester O-ethyl ester(1370229-72-3)

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: 1370229-72-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1370229-72-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,0,2,2 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1370229-72:
(9*1)+(8*3)+(7*7)+(6*0)+(5*2)+(4*2)+(3*9)+(2*7)+(1*2)=143
143 % 10 = 3
So 1370229-72-3 is a valid CAS Registry Number.

1370229-72-3Upstream product

1370229-72-3Downstream Products

1370229-89-2 5-(2-acetylamino-4,6-dimethoxyphenyl)piperidin-2-one

1370229-72-3Relevant academic research and scientific papers

Desulfonylative radical ring closure onto aromatics. A modular route to benzazepin-2-ones and 5-arylpiperidin-2-ones

Charrier, Nicolas,Liu, Zhibo,Zard, Samir Z.

, p. 2018 - 2021 (2012/06/01)

Adducts from the intermolecular radical addition of N-xanthylacetyl-N- methanesulfanilides to Boc-protected allylamine undergo ring closure with loss of a methanesulfonyl radical to give benzazepin-2-ones. Upon deprotection and exposure to triethylamine,

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