Cas 1393098-78-6,4-[(1-hydroxymethyl)-2-oxindolin-3-ylideneamino]-N-(5-methylisoxazol-3-yl)benzenesulphonamide

1393098-78-6

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Basic information

Product Name: 4-[(1-hydroxymethyl)-2-oxindolin-3-ylideneamino]-N-(5-methylisoxazol-3-yl)benzenesulphonamide
Synonyms:
CAS NO:1393098-78-6
Molecular Formula:
Molecular Weight: 412.426
EINECS: N/A
Product Categories: N/A
Mol File: 1393098-78-6.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: 4-[(1-hydroxymethyl)-2-oxindolin-3-ylideneamino]-N-(5-methylisoxazol-3-yl)benzenesulphonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-[(1-hydroxymethyl)-2-oxindolin-3-ylideneamino]-N-(5-methylisoxazol-3-yl)benzenesulphonamide(1393098-78-6)
EPA Substance Registry System: 4-[(1-hydroxymethyl)-2-oxindolin-3-ylideneamino]-N-(5-methylisoxazol-3-yl)benzenesulphonamide(1393098-78-6)

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: 1393098-78-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1393098-78-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,0,9 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1393098-78:
(9*1)+(8*3)+(7*9)+(6*3)+(5*0)+(4*9)+(3*8)+(2*7)+(1*8)=196
196 % 10 = 6
So 1393098-78-6 is a valid CAS Registry Number.

1393098-78-6Upstream product

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1393098-78-6Relevant articles and documents

Synthesis, characterization and in vitro antimicrobial evaluation of new compounds incorporating oxindole nucleus

Kandile, Nadia G.,Zaky, Howida T.,Mohamed, Mansoura I.,Ismaeel, Hind M.,Ahmed, Nashwa A.

experimental part, p. 599 - 608 (2012/09/08)

New compounds incorporating with the oxindole nucleus were synthesized via the reaction of substituted isatins [5-methyl-, 5-chloro- and 1-hydroxymethyl isatins] with different nucleophiles. The structures of the newly compounds were elucidated on the bas

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