Cas 1069086-93-6,2-(dimethylamino)ethyl 2-methyl-3-{[3-(morpholinocarbonyl)phenyl]sulfanyl}propanoate

1069086-93-6

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Basic information

Product Name: 2-(dimethylamino)ethyl 2-methyl-3-{[3-(morpholinocarbonyl)phenyl]sulfanyl}propanoate
Synonyms: 2-(dimethylamino)ethyl 2-methyl-3-{[3-(morpholinocarbonyl)phenyl]sulfanyl}propanoate
CAS NO:1069086-93-6
Molecular Formula:
Molecular Weight: 380.508
EINECS: N/A
Product Categories: N/A
Mol File: 1069086-93-6.mol
Article Data: 1

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: 2-(dimethylamino)ethyl 2-methyl-3-{[3-(morpholinocarbonyl)phenyl]sulfanyl}propanoate(CAS DataBase Reference)
NIST Chemistry Reference: 2-(dimethylamino)ethyl 2-methyl-3-{[3-(morpholinocarbonyl)phenyl]sulfanyl}propanoate(1069086-93-6)
EPA Substance Registry System: 2-(dimethylamino)ethyl 2-methyl-3-{[3-(morpholinocarbonyl)phenyl]sulfanyl}propanoate(1069086-93-6)

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: 1069086-93-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1069086-93-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,9,0,8 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1069086-93:
(9*1)+(8*0)+(7*6)+(6*9)+(5*0)+(4*8)+(3*6)+(2*9)+(1*3)=176
176 % 10 = 6
So 1069086-93-6 is a valid CAS Registry Number.

1069086-93-6Upstream product

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1069086-93-6Relevant articles and documents

Development of a tandem base-catalyzed, triphenylphosphine-mediated disulfide reduction-Michael addition

Bartolozzi, Alessandra,Foudoulakis, Hope M.,Cole, Bridget M.

experimental part, p. 2023 - 2032 (2009/04/03)

A tandem disulfide reduction-Michael addition was developed using both free and polymer-bound triphenylphosphine as the reducing agent. The procedure was applied to intermolecular systems for the synthesis of arylsulfanyl- and alkylsulfanyl-substi-tuted p

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