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244-50-8

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244-50-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 244-50-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,4 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 244-50:
(5*2)+(4*4)+(3*4)+(2*5)+(1*0)=48
48 % 10 = 8
So 244-50-8 is a valid CAS Registry Number.

244-50-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,8-diazafluorene

1.2 Other means of identification

Product number -
Other names 9H-Cyclopenta[1,2-b:4,3-b']dipyridine(7CI,8CI,9CI)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:244-50-8 SDS

244-50-8Downstream Products

244-50-8Relevant articles and documents

α,α-disubstituted aromatics and heteroaromatics as cognition enhancers

-

, (2008/06/13)

Cognitive defeciencies or neurological dysfunction in mammals are treated with α,α-disubstituted aromatic or heteroaromatic compounds. The compounds have the formula: STR1 or a salt thereof wherein X and Y are taken together to form a saturated or unsaturated carbocyclic or heterocyclic first ring and the shown carbon in said ring is α to at least one additional aromatic ring or heteroaromatic ring fused to the first ring; one of Het1 is 2, 3 or 4-pyridyl or 2, 4, or 5-pyrimidinyl and the other is selected from (a) 2, 3, or 4-pyridyl, (b) 2, 4, or 5-pyrimidinyl, (c) 2-pyrazinyl, (d) 3, or 4-pyridazinyl, (e) 3, or 4-pyrazolyl, (f) 2, or 3-tetrahydrofuranyl, and (g) 3-thienyl.

REACTIONS OF AZAFLUORENONES WITH HYDRAZINE

Mlochowski, Jacek,Szulc, Zdzislaw

, p. 33 - 39 (2007/10/02)

Formation and transformations of hydrazones, phenylhydrazones and azines, azafluorenone derivatives, have been studied and the influence of positions of heterocyclic nitrogen atoms on the reduction mechanism discussed.An improved reduction method of azafluorenones to azafluorenes has been elaborated.

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