Cas 35510-89-5,N-(2,4-dichlorophenyl)-4-hydroxy-2-methyl-1,1-dioxo-1$l^{6},2-benzothiazine-3-carboxamide

35510-89-5

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Basic information

Product Name: N-(2,4-dichlorophenyl)-4-hydroxy-2-methyl-1,1-dioxo-1$l^{6},2-benzothiazine-3-carboxamide
Synonyms:
CAS NO:35510-89-5
Molecular Formula: C₁₆H₁₂Cl₂N₂O₄S
Molecular Weight: 399.2485
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: 1.645g/cm³
Refractive Index: 1.712
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-(2,4-dichlorophenyl)-4-hydroxy-2-methyl-1,1-dioxo-1$l^{6},2-benzothiazine-3-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2,4-dichlorophenyl)-4-hydroxy-2-methyl-1,1-dioxo-1$l^{6},2-benzothiazine-3-carboxamide(35510-89-5)
EPA Substance Registry System: N-(2,4-dichlorophenyl)-4-hydroxy-2-methyl-1,1-dioxo-1$l^{6},2-benzothiazine-3-carboxamide(35510-89-5)

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: 35510-89-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 35510-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,1 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35510-89:
(7*3)+(6*5)+(5*5)+(4*1)+(3*0)+(2*8)+(1*9)=105
105 % 10 = 5
So 35510-89-5 is a valid CAS Registry Number.

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35510-89-5Relevant academic research and scientific papers

New Efficient Eco-Friendly Supported Catalysts for the Synthesis of Amides with Antioxidant and Anti-Inflammatory Properties

Charlet, Rogatien,Da?ch, Adam,Dufrénoy, Pierrick,Ghinet, Alina,Hechelski, Marie,Jawhara, Samir,Waterlot, Christophe

, (2020/02/20)

A new environmentally friendly approach for the synthesis of idrocilamide (1), a marketed myorelaxant and anti-inflammatory agent, is reported herein. The synthetic strategy involves a solvent-free aminolysis reaction catalyzed by zinc-containing species

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