Cas 5653-08-7,2-(3,4-dichlorophenyl)-4,4,7,8-tetramethyl-4,5-dihydro[1,2]thiazolo[5,4-c]quinoline-1(2H)-thione

5653-08-7

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Basic information

Product Name: 2-(3,4-dichlorophenyl)-4,4,7,8-tetramethyl-4,5-dihydro[1,2]thiazolo[5,4-c]quinoline-1(2H)-thione
Synonyms: 2-(3,4-Dichlorophenyl)-4,4,7,8-tetramethyl-4,5-dihydro[1,2]thiazolo[5,4-c]quinoline-1(2H)-thione; Isothiazolo[5,4-c]quinoline-1(2H)-thione, 2-(3,4-dichlorophenyl)-4,5-dihydro-4,4,7,8-tetramethyl-
CAS NO:5653-08-7
Molecular Formula: C₂₀H₁₈Cl₂N₂S₂
Molecular Weight: 421.4063
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 587.6°C at 760 mmHg
Flash Point: 309.2°C
Appearance: N/A
Density: 1.45g/cm³
Vapor Pressure: 8.69E-14mmHg at 25°C
Refractive Index: 1.732
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-(3,4-dichlorophenyl)-4,4,7,8-tetramethyl-4,5-dihydro[1,2]thiazolo[5,4-c]quinoline-1(2H)-thione(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3,4-dichlorophenyl)-4,4,7,8-tetramethyl-4,5-dihydro[1,2]thiazolo[5,4-c]quinoline-1(2H)-thione(5653-08-7)
EPA Substance Registry System: 2-(3,4-dichlorophenyl)-4,4,7,8-tetramethyl-4,5-dihydro[1,2]thiazolo[5,4-c]quinoline-1(2H)-thione(5653-08-7)

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: 5653-08-7(Hazardous Substances Data)

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5653-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5653-08-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5653-08:
(6*5)+(5*6)+(4*5)+(3*3)+(2*0)+(1*8)=97
97 % 10 = 7
So 5653-08-7 is a valid CAS Registry Number.

5653-08-7Upstream product

5653-60-1 3,3',4,4'-tetramethoxybenzoin

5653-08-7Downstream Products

5653-08-7Relevant academic research and scientific papers

Azole derivatives

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, (2008/06/13)

Azole derivatives of the formula SPC1 Wherein R1 is free or esterified carboxyl or other functionally modified carboxyl group, R2 and R3 each are aryl; A is Cn H2n in which n is an integer from 1 to 10, inclusive; and Z is O or S; and the physiologically acceptable salts thereof, possess, with good compatibility, excellent antiphlogistic activity and, in particular, influence favorably the chronic progressive diseases of the joints, e.g., arthritis. They can be prepared from compounds of the formula SPC2 Wherein X1 is a group convertible into the group --S--A--R1, and R2 and R3 have the values given above.

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