Cas 1260400-76-7,4-(1,3-benzothiazol-2-ylsulfanylmethyl)-2-(2,5-dichlorophenyl)-3-methyl-6,7-dihydro-2H-pyrazolo[3,4-d]pyridazin-7-one

1260400-76-7

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Basic information

Product Name: 4-(1,3-benzothiazol-2-ylsulfanylmethyl)-2-(2,5-dichlorophenyl)-3-methyl-6,7-dihydro-2H-pyrazolo[3,4-d]pyridazin-7-one
Synonyms:
CAS NO:1260400-76-7
Molecular Formula:
Molecular Weight: 474.394
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: 4-(1,3-benzothiazol-2-ylsulfanylmethyl)-2-(2,5-dichlorophenyl)-3-methyl-6,7-dihydro-2H-pyrazolo[3,4-d]pyridazin-7-one(CAS DataBase Reference)
NIST Chemistry Reference: 4-(1,3-benzothiazol-2-ylsulfanylmethyl)-2-(2,5-dichlorophenyl)-3-methyl-6,7-dihydro-2H-pyrazolo[3,4-d]pyridazin-7-one(1260400-76-7)
EPA Substance Registry System: 4-(1,3-benzothiazol-2-ylsulfanylmethyl)-2-(2,5-dichlorophenyl)-3-methyl-6,7-dihydro-2H-pyrazolo[3,4-d]pyridazin-7-one(1260400-76-7)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1260400-76-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1260400-76-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,4,0 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1260400-76:
(9*1)+(8*2)+(7*6)+(6*0)+(5*4)+(4*0)+(3*0)+(2*7)+(1*6)=107
107 % 10 = 7
So 1260400-76-7 is a valid CAS Registry Number.

1260400-76-7Upstream product

1260400-40-5 ethyl 4-[2-(1,3-benzothiazol-2-ylsulfanyl)-1-oxoethyl]-1-(2,5-dichlorophenyl)-5-methyl-1H-pyrazole-3-carboxylate

1260400-76-7Downstream Products

1260400-76-7Relevant academic research and scientific papers

Synthesis of 2-Aryl-4-(R-sulfanylmethyl)-3-methyl-6,7-dihydro-2H- pyrazolo[3,4-d]pyridazin-7-ones

Matiichuk,Potopnyk,Obushak

experimental part, p. 1550 - 1557 (2011/02/23)

Bromination of ethyl 1-aryl-4-acetyl-5-methyl-1H-pyrazole-3-carboxylates gave ethyl 1-aryl-4-(bromoacetyl)-5-methyl-1H-pyrazol-3-carboxylates which were used to alkylate benzenethiol and heterocyclic thiones at the sulfur atom. Reactions of the resulting

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