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42996-88-3

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42996-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42996-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,9,9 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 42996-88:
(7*4)+(6*2)+(5*9)+(4*9)+(3*6)+(2*8)+(1*8)=163
163 % 10 = 3
So 42996-88-3 is a valid CAS Registry Number.

42996-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-allyl-4-hydroxy-2-oxo-1,2-dihydroquinoline

1.2 Other means of identification

Product number -
Other names 3-Allyl-4-hydroxyquinolin-2(1H)-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:42996-88-3 SDS

42996-88-3Relevant articles and documents

An unusual condensation of alkyl 3-oxo-4-(triphenylarsoranylidene)butanoate with aldehydes; synthesis of symmetrical substituted 1,3,5-cycloheptatrienes

Moorhoff, Cornelis M.

, p. 4157 - 4160 (1997)

The unique preparation of 2-substituted 4,7-dihydroxycyclohepta-3,5,7-triene-1,3- dicarboxylates 5 from aldehydes 4 and two equivalents alkyl 3-oxo-4-(triphenylarsoranylidene)butanoate 3 is described.

Candida Rugosa lipase-catalyzed kinetic resolution of β-hydroxy- β-arylpropionates and δ-hydroxy-δ-aryl-β-oxo-pentanoates

Xu, Chengfu,Yuan, Chengye

, p. 2169 - 2186 (2007/10/03)

A simple and convenient method was reported for the preparation of optically active β-hydroxy-β-arylpropionates, δ-hydroxy-δ- aryl-β-oxo-pentanoates and their butyryl derivatives via CRL-catalyzed hydrolysis. The optically active products are potential precursors of some chiral pharmaceuticals and natural products.

Cumulated Ylides, 22. - Reactions of (Triphenylphosphoranylidene)ethenone with Halogen Compounds and their Preparative Application

Bestmann, Hans Juergen,Geismann, Christian,Zimmermann, Reiner

, p. 1501 - 1510 (2007/10/02)

(Triphenylphosphoranylidene)ethenone (6) reacts with halogen compounds 7 to yield four-membered ylide phosphonium salts 9.Ring opening of 9 under different conditions gives rise to the formation of bis-ylides 13, ylide salts 14, or bis-phosphonium salts 1

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