Cas 470476-92-7,ethyl {N-[3-chloro-4-(1-methylpiperidin-4-yloxy)phenyl]sulfamoyl}acetate

470476-92-7

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Basic information

Product Name: ethyl {N-[3-chloro-4-(1-methylpiperidin-4-yloxy)phenyl]sulfamoyl}acetate
Synonyms: ethyl {N-[3-chloro-4-(1-methylpiperidin-4-yloxy)phenyl]sulfamoyl}acetate
CAS NO:470476-92-7
Molecular Formula:
Molecular Weight: 390.888
EINECS: N/A
Product Categories: N/A
Mol File: 470476-92-7.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: ethyl {N-[3-chloro-4-(1-methylpiperidin-4-yloxy)phenyl]sulfamoyl}acetate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl {N-[3-chloro-4-(1-methylpiperidin-4-yloxy)phenyl]sulfamoyl}acetate(470476-92-7)
EPA Substance Registry System: ethyl {N-[3-chloro-4-(1-methylpiperidin-4-yloxy)phenyl]sulfamoyl}acetate(470476-92-7)

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: 470476-92-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 470476-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,0,4,7 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 470476-92:
(8*4)+(7*7)+(6*0)+(5*4)+(4*7)+(3*6)+(2*9)+(1*2)=167
167 % 10 = 7
So 470476-92-7 is a valid CAS Registry Number.

470476-92-7Upstream product

55896-93-0 ethyl 2-(chlorosulfonyl)acetate

470476-92-7Downstream Products

470476-92-7Relevant articles and documents

Discovery of R-142086 as a factor Xa (FXa) inhibitor: Syntheses and structure-activity relationships of cinnamyl derivatives1,2

Noguchi, Tetsuji,Tanaka, Naoki,Nishimata, Toyoki,Goto, Riki,Hayakawa, Miho,Sugidachi, Atsuhiro,Ogawa, Taketoshi,Niitsu, Yoichi,Asai, Fumitoshi,Ishizuka, Tomoko,Fujimoto, Koichi

experimental part, p. 22 - 33 (2009/08/07)

To develop a novel and effective anticoagulant with potent and selective factor Xa (FXa) inhibitory activity, a new series of cinnamyl derivatives with enhanced lipophilicity and prodrug forms were synthesized and their biological activities were evaluate

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