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Benzoxazole, 2-(2-benzothiazolylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77854-59-2

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77854-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77854-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,5 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77854-59:
(7*7)+(6*7)+(5*8)+(4*5)+(3*4)+(2*5)+(1*9)=182
182 % 10 = 2
So 77854-59-2 is a valid CAS Registry Number.

77854-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,3-benzothiazol-2-ylmethyl)-1,3-benzoxazole

1.2 Other means of identification

Product number -
Other names HMS1787G07

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:77854-59-2 SDS

77854-59-2Downstream Products

77854-59-2Relevant academic research and scientific papers

From bis(Imidazol-2-yl)methanes to asymmetrically substituted bis(heterocyclo)methanides in metal coordination

Dauer, David-R.,Koehne, Ingo,Herbst-Irmer, Regine,Stalke, Dietmar

, p. 1966 - 1978 (2017/12/06)

As an extension to the known symmetric bis(heterocyclmethanes containing two identical heterocycles, new asymmetric ligand systems, based on benzoxazole, benzothiazole and 1-methylbenzimidazole, are presented. Furthermore, the syntheses and reactions of two new symmetrically substituted methane derivatives, containing either 1-methylimidazole or 1-methylbenzimidazole, are discussed. In this context, firstly, (1-MeNCNC2H2)2CH2 and (1-MeNCNC6H4)2CH2, and secondly, (NCSC6H4)CH2(NCOC6H4) and (NCSC6H4)CH2(1-MeNCNC6H4), are used as parent compounds. They can be easily deprotonated at the central methylene bridge to generate a monoanionic structure akin to NacNac, so that the following complexes can be obtained: [Me2Al{(1-MeNCNC2H2)2CH}], [Me2Al{(1-MeNCNC6H4)2-CH}], [Me2Al{(NCSC6H4)CH(NCOC6H4)}], [Me2Ga{(NCSC6H4)CH-(NCOC6H4)}], [Me2Al{(NCSC6H4)CH(1-MeNCNC6H4)}],[(THF)2Li{(1-MeNCNC6H4)2CH}] and [(diox)2Li{(NCSC6H4)CH(1-MeNCNC6H4)}]. These compounds have been fully characterised by single-crystal X-ray diffraction (in the solid statand NMR spectroscopy (in solution).

Rhodium-catalyzed synthesis of unsymmetrical di(aryl/heteroaryl)methanes using aryl/heteroarylmethyl ketones via CO-C bond cleavage

Li, Guangzhe,Arisawa, Mieko,Yamaguchi, Masahiko

supporting information, p. 4328 - 4330 (2014/04/17)

RhH(PPh3)4 and 1,2-bis(diphenylphosphino)benzene catalyze the reaction of aryl/heteroarylmethyl ketones and aryl heteroaryl ethers giving unsymmetrical diarylmethanes containing one or two heteroarenes in high yields. The reaction do

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