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70292-64-7

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70292-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70292-64-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,2,9 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70292-64:
(7*7)+(6*0)+(5*2)+(4*9)+(3*2)+(2*6)+(1*4)=117
117 % 10 = 7
So 70292-64-7 is a valid CAS Registry Number.

70292-64-7SDS

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 2-ethoxy-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 2-ethoxybenzothiazole

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:70292-64-7 SDS

70292-64-7Relevant articles and documents

Cs2CO3-Promoted C?O Coupling Protocol Enables Solventless (Hetero)aryl Ether Synthesis under Air Atmosphere

Jiang, Bowen,Chen, Cheng,Fan, Guang-Gao,Sang, Wei,Cheng, Hua,Zhang, Rui,Yuan, Ye,Li, Qi-Zhong,Verpoort, Francis

supporting information, (2022/02/05)

In this work, a Cs2CO3-promoted synthetic approach was identified for (hetero)aryl ether synthesis via the C?O coupling of various (hetero)aryl chlorides and alcohols/phenol. To our delight, the reactions could be carried out under transition-metal-free and solvent-free conditions. Moreover, analytical-grade reagents and air atmosphere were readily tolerated. To showcase the practical usefulness of the present protocol, the assembly of a bioactive molecule was facilely realized and the gram-scale production of selected ether products was also efficiently accomplished. In addition, density functional theory (DFT) studies, along with a few mechanistic experiments, were conducted to elucidate a proposed reaction pathway and rationalize the pivotal role of Cs2CO3 in promoting this process. Hopefully, this work could provide useful information for researchers who are engaging in C?O cross-coupling reactions.

Copper(I)-catalyzed cascade synthesis of 2-substituted 1,3-benzothiazoles: Direct access to benzothiazolones

Murru, Siva,Mondal, Pravat,Yella, Ramesh,Patel, Bhisma K.

experimental part, p. 5406 - 5413 (2010/02/28)

An efficient cascade process for the preparation of 2-substituted 1,3-benzothiazoles directly from 2-haloaryl isothiocyanates and O or S nucleophiles by a Cu-catalyzed, intramolecular, C-S bond formation has been developed. This cascade method is viable f

Process for synthesizing thiacyanine dyes

-

, (2008/06/13)

There is described a process for synthesizing a thiacyanine dye wherein a 2-halo, 2-alkoxy or 2-aryloxybenzothiazole is alkylated by a strong alkylating agent to form a quaternized benzothiazole which, without being isolated, is condensed with a benzothiazolium betaine in a nonaqueous homogeneous medium. The thiacyanine dye is useful for enhancing the photosensitivity of a blue-sensitive silver halide emulsion.

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