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27820-27-5

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27820-27-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27820-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,2 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27820-27:
(7*2)+(6*7)+(5*8)+(4*2)+(3*0)+(2*2)+(1*7)=115
115 % 10 = 5
So 27820-27-5 is a valid CAS Registry Number.

27820-27-5SDS

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 2-(4-bromo-phenyl)-indol-3-one-1-oxide

1.2 Other means of identification

Product number -
Other names 2-(4-Bromo-phenyl)-1-oxy-indol-3-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:27820-27-5 SDS

27820-27-5Downstream Products

27820-27-5Relevant articles and documents

C-H alkenylation/cyclization and sulfamidation of 2-phenylisatogens using: N -oxide as a directing group

Guo, Lingmei,Tang, Baolan,Nie, Ruifang,Liu, Yanzhao,Lv, Shan,Wang, Huijing,Guo, Li,Hai, Li,Wu, Yong

supporting information, p. 10623 - 10626 (2019/09/06)

The first example of transition-metal-catalyzed C-H activations of 2-phenylisatogens with alkynes and sulfonyl azides has been developed using N-oxide as the directing group. Ru(ii)-Catalyzed C-H alkenylation/cyclization and Ir(iii)-catalyzed direct C-H sulfamidation proceeded with good yields and excellent functional group tolerance. Importantly, these two transformations provided straightforward routes for the synthesis of indol-3-one derivatives and sulfamidated 2-phenylisatogens respectively, which might be of considerable bioactivities.

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