Cas 212622-39-4,4-[5-Bromo-1-(1,1-dibromo-2-oxo-propyl)-6-oxo-1,6-dihydro-pyridazin-4-yloxy]-benzonitrile

212622-39-4

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Basic information

Product Name: 4-[5-Bromo-1-(1,1-dibromo-2-oxo-propyl)-6-oxo-1,6-dihydro-pyridazin-4-yloxy]-benzonitrile
Synonyms: 4-[5-Bromo-1-(1,1-dibromo-2-oxo-propyl)-6-oxo-1,6-dihydro-pyridazin-4-yloxy]-benzonitrile
CAS NO:212622-39-4
Molecular Formula:
Molecular Weight: 505.948
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-[5-Bromo-1-(1,1-dibromo-2-oxo-propyl)-6-oxo-1,6-dihydro-pyridazin-4-yloxy]-benzonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 4-[5-Bromo-1-(1,1-dibromo-2-oxo-propyl)-6-oxo-1,6-dihydro-pyridazin-4-yloxy]-benzonitrile(212622-39-4)
EPA Substance Registry System: 4-[5-Bromo-1-(1,1-dibromo-2-oxo-propyl)-6-oxo-1,6-dihydro-pyridazin-4-yloxy]-benzonitrile(212622-39-4)

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: 212622-39-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 212622-39-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,6,2 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 212622-39:
(8*2)+(7*1)+(6*2)+(5*6)+(4*2)+(3*2)+(2*3)+(1*9)=94
94 % 10 = 4
So 212622-39-4 is a valid CAS Registry Number.

212622-39-4Upstream product

212622-39-4Downstream Products

212622-49-6 5-bromo-4-(4-cyanophenoxy)pyridazin-6-one

212622-39-4Relevant academic research and scientific papers

Functionalization of 4,5-Dihalopyridazin-6-ones Using 1-(1,1-Dibromo-2-oxopropyl) Derivatives

Kang, Young-Jin,Chung, Hyun-A,Kweon, Deok-Heon,Cho, Su-Dong,Lee, Sang-Gyeong,Kim, Sung-Kyu,Yoon, Yong-Jin

, p. 595 - 600 (1998)

Functionalization of 4,5-dihalopyridazin-6-ones using 1-(1,1-dibromo-2-oxopropyl)-4,5-dihalopyridazin-6-ones with some nucleophiles gave regioselectively only 5-halo-4-substituted-pyridazin-6-ones.

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