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53983-76-9

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53983-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53983-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,8 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53983-76:
(7*5)+(6*3)+(5*9)+(4*8)+(3*3)+(2*7)+(1*6)=159
159 % 10 = 9
So 53983-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C24H19NO/c26-22-16-15-19-11-7-8-14-21(19)23(22)24(20-12-5-2-6-13-20)25-17-18-9-3-1-4-10-18/h1-17,24,26H/b25-17+

53983-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(benzylideneamino)-phenylmethyl]naphthalen-2-ol

1.2 Other means of identification

Product number -
Other names -

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:53983-76-9 SDS

53983-76-9Relevant articles and documents

Synthesis of 1-(α-Aminobenzyl)-2-naphthol derivatives, their structure in crystal and in solution

Metlushka,Sadkova,Shaimardanova,Tufatullin,Zheltukhin,Kataeva,Alfonsov

, p. 80 - 85 (2015/01/30)

The series of tautomeric 1,3-diarylnaphthoxazines (the Betti base precursors) was obtained by the interaction of 2-naphthols and 1,3,5-trisaryl-2,4-diazapenta-1,4-dienes. Their structure has been established in solid state and solution.

Efficient synthesis of naphtho[1,2-e][1,3]oxazine derivatives via a chemoselective reaction with the aid of low-valent titanium reagent

Shi, Daqing,Rong, Shaofeng,Dou, Guolan,Wang, Manman

scheme or table, p. 25 - 30 (2010/10/03)

A series of new naphtho[1,2-e][1,3]oxazine derivatives such as trans-1,3-diaryl-1H-naphtho[1,2-e][1,3]oxazine-2(3H)-carbonyl chloride, 1-aryl-2-benzyl-1,2- dihydronaphtho[1,2-e][1,3]oxazine-3-one, and trans-1,3-diaryl-1H-naphtho[1,2-e] [1,3]oxazine-2(3H)-

1-(a-Aminobenzyl)-2-naphthol: A new chiral auxiliary for the synthesis of enantiopure a-aminophosphonic acids

Metlushka, Kirill E.,Kashemirov, Boris A.,Zheltukhin, Viktor F.,Sadkova, Dilyara N.,Buechner, Bernd,Hess, Christian,Kataeva, Olga N.,McKenna, Charles E.,Alfonsov, Vladimir A.

supporting information; experimental part, p. 6718 - 6722 (2010/02/28)

A new diastereoselective synthesis of a-aminophosphonates has been developed, based on the reaction, in the presence of trifluoroacetic acid, of trialkyl phosphites with chiral imines derived from (R)- or (S)-l-(ot- aminobenzyl)-2-naphthol. The reaction p

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