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1011455-82-5

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1011455-82-5 Usage

General Description

Benzothiazol-2-yl-piperidin-4-ol is a chemical compound with a molecular formula C12H14N2OS and a molecular weight of 234.32 g/mol. It is known for its high purity, typically at 98% or greater. Benzothiazol-2-yl-piperidin-4-ol, 98+% C12H14N2OS, MW: 234.32 belongs to the class of organic compounds known as phenothiazines and is commonly used in pharmaceutical and research applications. It is a versatile building block in organic synthesis, and its unique structure and properties make it valuable in the development of various drugs and pharmaceutical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1011455-82-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,1,4,5 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1011455-82:
(9*1)+(8*0)+(7*1)+(6*1)+(5*4)+(4*5)+(3*5)+(2*8)+(1*2)=95
95 % 10 = 5
So 1011455-82-5 is a valid CAS Registry Number.

1011455-82-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1,3-Benzothiazol-2-yl)-4-piperidinol

1.2 Other means of identification

Product number -
Other names 1-benzothiazol-2-yl-piperidin-4-ol

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:1011455-82-5 SDS

1011455-82-5Downstream Products

1011455-82-5Relevant articles and documents

Dioxygen-triggered oxidative cleavage of the C-S bond towards C-N bond formation

Lv, Zongchao,Wang, Huamin,Quan, Zhicong,Gao, Yuan,Lei, Aiwen

, p. 12332 - 12335 (2019)

Research on the cleavage of C-C bonds has been well developed. By comparison with this, the activation of C-S bonds remains challenging. Herein, dioxygen-triggered oxidative cleavage of C-S bonds has been achieved, delivering a series of N-containing heterocyclic compounds that are frequently found in pesticides and pharmaceuticals. Additionally, the potential utility of this protocol was further demonstrated by a gram-scale experiment. Mechanistically, dioxygen plays a key role in the cleavage of C-S bonds towards C-N bond formation.

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