Cas 1581-03-9,2-amino-4-trifluoromethyl-2',4'-dinitrodiphenylsulfide

1581-03-9

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Basic information

Product Name: 2-amino-4-trifluoromethyl-2',4'-dinitrodiphenylsulfide
Synonyms: 2-amino-4-trifluoromethyl-2',4'-dinitrodiphenylsulfide
CAS NO:1581-03-9
Molecular Formula:
Molecular Weight: 359.285
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: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-amino-4-trifluoromethyl-2',4'-dinitrodiphenylsulfide(CAS DataBase Reference)
NIST Chemistry Reference: 2-amino-4-trifluoromethyl-2',4'-dinitrodiphenylsulfide(1581-03-9)
EPA Substance Registry System: 2-amino-4-trifluoromethyl-2',4'-dinitrodiphenylsulfide(1581-03-9)

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: 1581-03-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1581-03-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,8 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1581-03:
(6*1)+(5*5)+(4*8)+(3*1)+(2*0)+(1*3)=69
69 % 10 = 9
So 1581-03-9 is a valid CAS Registry Number.

1581-03-9Upstream product

1581-03-9Downstream Products

2069-32-1 7-nitro-2-(trifluoromethyl)phenothiazine

1581-03-9Relevant academic research and scientific papers

SYNTHESIS OF SOME SUBSTITUTED 8-TRIFLUOROMETHYLNITROPHENOTHIAZINES

Malik, Seema,Anand, Madhu,Verma, S. S.,Prakash, L.,Mital, R. L.

, p. 201 - 214 (1989)

The synthesis of variedly ring substituted phenothiazines with two strong electron-withdrawing groups (trifluoromethyl and nitro) have been accomplished by the reactions of some reactive halonitrobenzenes with the zinc mercaptide of 2-amino-4-trifluoromethylbenzenethiol.The products have been characterised by elemental analysis, IR, 1H, 19F NMR and mass spectral studies.

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