Cas 83749-69-3,4-(4-Bromo-phenyl)-2,5-dihydro-pyridazino[4,5-b]indol-1-one

83749-69-3

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Basic information

Product Name: 4-(4-Bromo-phenyl)-2,5-dihydro-pyridazino[4,5-b]indol-1-one
Synonyms: 4-(4-Bromo-phenyl)-2,5-dihydro-pyridazino[4,5-b]indol-1-one
CAS NO:83749-69-3
Molecular Formula:
Molecular Weight: 340.179
EINECS: N/A
Product Categories: N/A
Mol File: 83749-69-3.mol
Article Data: 1

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-(4-Bromo-phenyl)-2,5-dihydro-pyridazino[4,5-b]indol-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 4-(4-Bromo-phenyl)-2,5-dihydro-pyridazino[4,5-b]indol-1-one(83749-69-3)
EPA Substance Registry System: 4-(4-Bromo-phenyl)-2,5-dihydro-pyridazino[4,5-b]indol-1-one(83749-69-3)

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: 83749-69-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 83749-69-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,4 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83749-69:
(7*8)+(6*3)+(5*7)+(4*4)+(3*9)+(2*6)+(1*9)=173
173 % 10 = 3
So 83749-69-3 is a valid CAS Registry Number.

83749-69-3Upstream product

75822-51-4 2-(4-Bromo-benzoyl)-1H-indole-3-carboxylic acid

83749-69-3Downstream Products

83749-80-8 4-(4-Bromo-phenyl)-1-chloro-5H-pyridazino[4,5-b]indole

83749-69-3Relevant articles and documents

SYNTHESIS OF 5H-PYRIDAZOINDOLES BY CONDENSATION OF 2-ACYLINDOLE-3-CARBOXYLIC ACIDS WITH HYDRAZINE

Zhungietu, G. I.,Zorin, L. M.,Gorgos, V. I.,Rekhter, M. A.

, p. 811 - 813 (1982)

5H-Pyridazoindol-1-ones were obtained by heating 2-acetylindole-3- or 2-aroylindole-3-carboxylic acids with hydrazine hydrate in ethylene glycol or alcohol. 1-Chloro-5H-pyridazoindoles are formed by treatment of 5H-pyridazoindol-1-one

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