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17931-24-7

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17931-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17931-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,3 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17931-24:
(7*1)+(6*7)+(5*9)+(4*3)+(3*1)+(2*2)+(1*4)=117
117 % 10 = 7
So 17931-24-7 is a valid CAS Registry Number.

17931-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3H-benzo[g][1,3]benzothiazol-2-one

1.2 Other means of identification

Product number -
Other names Naphtho-2',1':4,5-thiazolon

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:17931-24-7 SDS

17931-24-7Downstream Products

17931-24-7Relevant articles and documents

Transition-metal-free synthesis of thiazolidin-2-ones and 1,3-thiazinan-2-ones from arylamines, elemental sulfur and CO2

Ran, Chuan-Kun,Song, Lei,Niu, Ya-Nan,Wei, Ming-Kai,Zhang, Zhen,Zhou, Xiao-Yu,Yu, Da-Gang

, p. 274 - 279 (2021)

Transfering waste to treasure is highly important in green chemistry. However, it is difficult to realize it efficiently due to the low reactivity, especially the simultaneous utilization of two unreactive feedstocks in one reaction. Herein, we report the first utilization of both elemental sulfur and CO2 in a multi-component reaction to generate valuable thiazolidin-2-ones and 1,3-thiazinan-2-ones. Under transition-metal-free reaction conditions, a variety of easily available arylamines react with elemental sulfur and CO2 (1 atm) to give functional thiazolidin-2-ones and 1,3-thiazinan-2-ones in moderate to good yields via C-H bond functionalization. This strategy is highlighted by high step economy with generation of three bonds in one reaction and good functional groups tolerance.

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