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91527-77-4

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91527-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91527-77-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,2 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 91527-77:
(7*9)+(6*1)+(5*5)+(4*2)+(3*7)+(2*7)+(1*7)=144
144 % 10 = 4
So 91527-77-4 is a valid CAS Registry Number.

91527-77-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3'-coumarinyl)-3-(4''-dimethylaminophenyl)-2-propen-1-one

1.2 Other means of identification

Product number -
Other names 3-(3-(4-dimethylaminophenyl)acryloyl)-2H-chromen-2-one

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:91527-77-4 SDS

91527-77-4Relevant articles and documents

The effects of bromine atoms on the photophysical and photochemical properties of 3-cinnamoylcoumarin derivatives

Sun, Zhiyuan,Wang, Yu,Fang, De-Cai,Zhao, Yuxia

, p. 7377 - 7382 (2018/05/07)

Eight coumarin derivatives (T1-T8) with or without modification using one or two bromine atoms were synthesized through the aldol condensation reaction. Their photophysical, photochemical and electrochemical properties were investigated. It was shown that

Synthesis and florescent properties of 5-aryl-3-(3-coumarinyl)-1-benzothiazolyl-2-pyrazolines

Liu, Manman,Liu, Qian,Zhang, Jian

, p. 301 - 306 (2016/08/20)

A series of novel 5-Aryl-3-(3-coumarinyl)-1-benzothiazolyl-2-pyrazolines have been synthesized by the reaction of 3-coumarinyl chalcones with 2-hydrazinobenzothiazole in hot ethanol. And the structures of these new compounds have been characterized by 1HNMR, MS and elemental analysis. The fluorescence spectra of these compounds were also measured. All the compounds showed up strong green light emissions (λem: 557-570nm). The results showed that the absorption maxima of the compound vary from 415 to 420nm depending on the group bonded to pyrazolines rings.

Antidiabetic effect of novel benzenesulfonylureas as PPAR-γ agonists and their anticancer effect

Kharbanda, Chetna,Alam, Mohammad Sarwar,Hamid, Hinna,Javed, Kalim,Dhulap, Abhijeet,Bano, Sameena,Ali, Yakub

, p. 4601 - 4605 (2015/10/12)

Twenty one pyrazoline containing benzenesulfonylureas were synthesized and docked against PPAR-γ target. All the compounds were first screened for their antidiabetic potential by oral glucose tolerance test and then six active compounds were assessed on S

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