Cas 333998-25-7,N-(2,2-dimethoxy-ethyl)-N-(4-methoxy-9H-xanthen-9-yl)-4-methyl-benzenesulfonamide

333998-25-7

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Basic information

Product Name: N-(2,2-dimethoxy-ethyl)-N-(4-methoxy-9H-xanthen-9-yl)-4-methyl-benzenesulfonamide
Synonyms: N-(2,2-dimethoxy-ethyl)-N-(4-methoxy-9H-xanthen-9-yl)-4-methyl-benzenesulfonamide
CAS NO:333998-25-7
Molecular Formula:
Molecular Weight: 469.558
EINECS: N/A
Product Categories: N/A
Mol File: 333998-25-7.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: N-(2,2-dimethoxy-ethyl)-N-(4-methoxy-9H-xanthen-9-yl)-4-methyl-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2,2-dimethoxy-ethyl)-N-(4-methoxy-9H-xanthen-9-yl)-4-methyl-benzenesulfonamide(333998-25-7)
EPA Substance Registry System: N-(2,2-dimethoxy-ethyl)-N-(4-methoxy-9H-xanthen-9-yl)-4-methyl-benzenesulfonamide(333998-25-7)

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: 333998-25-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 333998-25-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,3,9,9 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 333998-25:
(8*3)+(7*3)+(6*3)+(5*9)+(4*9)+(3*8)+(2*2)+(1*5)=177
177 % 10 = 7
So 333998-25-7 is a valid CAS Registry Number.

333998-25-7Upstream product

333998-25-7Downstream Products

333998-25-7Relevant articles and documents

[1]Benzopyrano[2,3,4-i,j]isoquinolines: A new, versatile route from 1-bromoxanthones

García, Alberto,Domínguez, Domingo

, p. 5219 - 5221 (2001)

[1]Benzopyrano[2,3,4-i,j]isoquinolines were synthesized from a bromoxanthone by assembly of the isoquinoline ring in three steps: vinylation, hydroamination and ring-closing reduction of the xanthone carbonyl.

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