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106058-73-5

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106058-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106058-73-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,5 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106058-73:
(8*1)+(7*0)+(6*6)+(5*0)+(4*5)+(3*8)+(2*7)+(1*3)=105
105 % 10 = 5
So 106058-73-5 is a valid CAS Registry Number.

106058-73-5SDS

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 3,3'-(phenylmethylene)bis(4-hydroxy-1-methylquinolin-2(1H)-one)

1.2 Other means of identification

Product number -
Other names 3,3'-benzylidenebis<4-hydroxy-1-methyl-2-quinolone>

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:106058-73-5 SDS

106058-73-5Downstream Products

106058-73-5Relevant articles and documents

Water-mediated, green, and efficient synthesis of bisquinolones under catalyst-free conditions

Madhu, Bandi,Reddy, Ch. Venkata Ramana,Dubey, Pramod Kumar

, p. 421 - 427 (2017)

Water-mediated, green, and efficient synthesis involving condensation of 4-hydroxy-1-methylquinoline-2(1H)-one (3) with different aromatic and heterocyclic aldehydes (4a–n) leading to 3,3′-(arylmethylene)-bis-(4-hydroxy-1-methylquinolin-2(1H)-one) 5(a–n) under catalyst-free conditions is described. This reaction has an easy workup without using column chromatography and provides excellent yields of the products in shorter reaction times. It does not require any catalyst and uses water as the medium which is the greenest solvent. 3 required in this work was itself obtained by condensation of N-methylaniline (1) with malonic acid (2) in the presence of POCl3using a previously reported procedure.

Synthesis of SF2809-V, chymase inhibitor, and its analogs by three component reaction: Model study for high throughput synthesis of a chymase inhibitor library

Yamamoto, Yasuo,Harimaya, Kenzo

, p. 238 - 239 (2004)

SF2809-V, chymase inhibitor, was synthesized by a three component reaction and its sixteen analogs were also synthesized to establish a method for preparation of a chymase inhibitor library.

DBU Acetate Mediated: One-pot Multi Component Syntheses of Dihydropyrano[3,2-c]quinolones

Bhupathi, Rajasekar,Madhu, Bandi,Devi, B. Rama,Reddy, Ch. Venkata Ramana,Dubey

, p. 1911 - 1916 (2016)

Three-component reaction involving condensation of 1-methylquinoline-2,4(1H,3H)-dione(1), aromatic aldehydes (2a, 2b, 2c, 2d, 2e, 2f, 2g, 2h) and malononitrile/cyanoaceticester (3a, 3b) in{(1,8-diazabicyclo[5.4.0]-undec-7-en-8-ium acetate)}[DBU][Ac] as ta

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