Cas 586956-85-6,2H-[1]Benzopyrano[4,3-d][1,2,3]thiadiazole, 3a-chloro-3a,4-dihydro-4,4-dimethyl-2-(4-nitrophenyl)-

586956-85-6

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Basic information

Product Name: 2H-[1]Benzopyrano[4,3-d][1,2,3]thiadiazole, 3a-chloro-3a,4-dihydro-4,4-dimethyl-2-(4-nitrophenyl)-
Synonyms:
CAS NO:586956-85-6
Molecular Formula: C17H14ClN3O3S
Molecular Weight: 375.835
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: 2H-[1]Benzopyrano[4,3-d][1,2,3]thiadiazole, 3a-chloro-3a,4-dihydro-4,4-dimethyl-2-(4-nitrophenyl)-(CAS DataBase Reference)
NIST Chemistry Reference: 2H-[1]Benzopyrano[4,3-d][1,2,3]thiadiazole, 3a-chloro-3a,4-dihydro-4,4-dimethyl-2-(4-nitrophenyl)-(586956-85-6)
EPA Substance Registry System: 2H-[1]Benzopyrano[4,3-d][1,2,3]thiadiazole, 3a-chloro-3a,4-dihydro-4,4-dimethyl-2-(4-nitrophenyl)-(586956-85-6)

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: 586956-85-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 586956-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,6,9,5 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 586956-85:
(8*5)+(7*8)+(6*6)+(5*9)+(4*5)+(3*6)+(2*8)+(1*5)=236
236 % 10 = 6
So 586956-85-6 is a valid CAS Registry Number.

586956-85-6Upstream product

586956-85-6Downstream Products

586956-85-6Relevant academic research and scientific papers

Synthesis of hindered hydrazones and their reaction with thionyl chloride

Hegab, Mohamed I.,Hassan, Nasser A.,El-Telbani, Emad M.,Ahmed Farag, Ibrahim S.,Abdel-Megeid, Farouk M.E.

, p. 223 - 228 (2007/10/03)

Hydrazones 12a-c and ketazines 13a-c were prepared by the reaction of ketones 11a-c with hydrazine hydrate depending on the temperature and the reaction time. Some ketone (aryl)hydrazone derivatives 14a,c,e reacted with thionyl chloride to afford the chlo

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