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107027-76-9

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107027-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107027-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,2 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107027-76:
(8*1)+(7*0)+(6*7)+(5*0)+(4*2)+(3*7)+(2*7)+(1*6)=99
99 % 10 = 9
So 107027-76-9 is a valid CAS Registry Number.

107027-76-9SDS

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 8-(methoxycarbonyl)-2-phenyl-4(1H)-quinolone

1.2 Other means of identification

Product number -
Other names 4-Oxo-2-phenyl-1,4-dihydro-quinoline-8-carboxylic acid methyl ester

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:107027-76-9 SDS

107027-76-9Relevant articles and documents

Substituted quinoline derivatives and pharmaceutical compositions thereof

-

, (2008/06/13)

The novel class of substituted quinolines represented by the general formula (I): STR1 where each of R1 and R2 separately represents H or up to three of the groups lower alkyl, halogen, CF3, CN, SO2 CH3, NO2, OH, NH2, NHSO2 R3, NHCOOR3, OR3, SR3, NHR3 or NR3 R3 (where R3 is lower alkyl optionally substituted with hydroxy, amino or ether functions), and each of R1 and R2 may additionally separately represent the substitution of an aza (--N=) group for one or two of the methine (--CH=) groups in each of the carbocyclic rings, and R1 may also represent, at positions 2', 3' or 4' only, a phenyl ring optionally further substituted with lower alkyl, halogen, CF3, CN, SO2 CH3, NO2, OH, NH2, NHCOR3, NHCOOR3, OR3, SR3, NHR3 or NR3 R3 (where R3 is lower alkyl optionally substituted with hydroxy, amino or ether functions); Y represents C(NH)NH2, NHC(NH)NH2 or NR4 R5, where each of R4 and R5 is H or lower alkyl optionally substituted with hydroxy, amino or ether functions, or R4 and R5 together with the nitrogen atom form a heterocyclic ring; and n is from 2 to 6; and the acid addition salts and 1-N-oxides thereof, possess antibacterial and antitumor properties.

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