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19430-24-1

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19430-24-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19430-24-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,3 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19430-24:
(7*1)+(6*9)+(5*4)+(4*3)+(3*0)+(2*2)+(1*4)=101
101 % 10 = 1
So 19430-24-1 is a valid CAS Registry Number.

19430-24-1SDS

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 2-(benzylideneamino)-4-methylphenol

1.2 Other means of identification

Product number -
Other names 2-(Benzylidenamino)-p-kresol

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:19430-24-1 SDS

19430-24-1Relevant articles and documents

Enantioselective Strecker and Allylation Reactions with Aldimines Catalyzed by Chiral Oxazaborolidinium Ions

Kang, Ki-Tae,Park, Sang Hyun,Ryu, Do Hyun

supporting information, p. 6679 - 6683 (2019/09/12)

Chiral oxazaborolidinium ion (COBI)-catalyzed enantioselective nucleophilic addition reactions of aldimines using tributyltin cyanide and allyltributylstannane have been developed. Various α-aminonitriles and homoallylic amines were synthesized in high yi

N-Heterocyclic Carbene (NHC)-Catalyzed One-Pot Aerobic Oxidative Synthesis of 2-Substituted Benzo[ d ]oxazoles, Benzo[ d ]thiazoles and 1,2-Disubstituted Benzo[ d ]imidazoles

Zhou, Quan,Liu, Shu,Ma, Ming,Cui, He-Zhen,Hong, Xi,Huang, Shuang,Zhang, Jing-Fan,Hou, Xiu-Feng

, p. 1315 - 1322 (2018/03/10)

N-Heterocyclic carbene (NHC), generated in situ from easily available N-heterocyclic imidazolium salt with air as terminal oxidant, has successfully been utilized as a cheap and efficient catalyst for one-pot aerobic oxidative synthesis of 2-arylbenzo[ d ]oxazoles, 2-substituted benzo[ d ]thiazoles, and 1,2-disubstituted benzo[ d ]imidazoles.

Aryl schiff base derivate and preparation method and application thereof

-

Paragraph 0026; 0027; 0028; 0029; 0030; 0031-0038, (2017/08/28)

The invention discloses an aryl schiff base derivate and preparation method and a preparation method and application thereof. The structural formula of the aryl schiff base derivate sees description. The preparation method is characterized in that a certa

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