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5847-63-2

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5847-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5847-63-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5847-63:
(6*5)+(5*8)+(4*4)+(3*7)+(2*6)+(1*3)=122
122 % 10 = 2
So 5847-63-2 is a valid CAS Registry Number.

5847-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-4-(2,3-diethoxyphenyl)-7-methyl-5-oxo-6-(2-phenylethyl)-4H-pyrano[3,2-c]pyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-chorostilbazole

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:5847-63-2 SDS

5847-63-2Relevant articles and documents

A new insight into the push-pull effect of substituents via the stilbene-like model compounds

Cao, Chaotun,Cao, Chenzhong,Zeng, Zhao

, (2022/02/01)

In this paper, authors report on 1-pyridyl-2-arylethenes, 1-furyl-2-arylethylenes, 1,2-diphenylpropylenes and substituted cinnamyl anilines as stilbene-like model compounds to investigate the factors dominating the push-pull effect of substituents via usi

Ligand-free palladium-catalysed oxidative Heck reaction of 4-vinylpyridine with arylboronic acids: Selective synthesis of (E)-4-styrylpyridines

Shi, Chuanli,Ding, Jinchang,Jiang, Jun,Chen, Jiuxi,Wu, Huayue,Liu, Miaochang

supporting information; experimental part, p. 322 - 325 (2012/09/21)

A ligand-free palladium-catalysed oxidative Heck reaction of various arylboronic acids with 4-vinylpyridine has been developed, achieving (E)-4-styrylpyridines with high selectively in moderate to good yields. A plausible mechanism for the formation of (E)-4-styrylpyridines has been proposed.

Electronic Interactions in Aromatic Compounds. Direct Electronic Interaction between Aromatic Rings in Conjugated and Non-Conjugated cis-Compounds

Mancini, Vittorio,Passini, Paolo,Santini, Sergio

, p. 463 - 466 (2007/10/02)

A study of charge transfer equilibria between a series of cis- and trans-4-styrylpyridines and cis- and trans-1-(4-X-phenyl)-2-(4-pyridyl)cyclopropanes with iodine has been carried out in CCl4.Acidity constants for these heteroaromatic compounds were determined.The results obtained for the two types of measurements show that through-space conjugation, due to overlap of the non-parallel ?-orbitals of the two aromatic systems, operated in both cis-systems.

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