1356342-15-8 Usage
White, crystalline solid
Describes the physical appearance of the compound.
Used in laboratory research as a reagent or building block
Indicates its common applications in scientific studies.
Potential as an anticancer agent
Highlights the compound's possible medical applications.
Active against hematological malignancies
Specifies the types of cancer the compound may be effective against.
Functions as a prodrug
Explains the mechanism of action of the compound in the body.
Promising results in preclinical studies
Indicates the current state of research on the compound's efficacy.
Further research needed to establish safety and efficacy in humans
Notes the limitations of current research and the need for additional studies.
Check Digit Verification of cas no
The CAS Registry Mumber 1356342-15-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,6,3,4 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1356342-15:
(9*1)+(8*3)+(7*5)+(6*6)+(5*3)+(4*4)+(3*2)+(2*1)+(1*5)=148
148 % 10 = 8
So 1356342-15-8 is a valid CAS Registry Number.
1356342-15-8Relevant articles and documents
Microwave-Enhanced On-Water Amination of 2-Mercaptobenzoxazoles to Prepare 2-Aminobenzoxazoles
Tankam, Theeranon,Srisa, Jakkrit,Sukwattanasinitt, Mongkol,Wacharasindhu, Sumrit
, p. 11936 - 11943 (2018/10/02)
In this work, we developed a catalyst-free amination of 2-mercaptobenzoxazoles on water under microwave irradiation. The product, 2-aminobenzoxazoles, was successfully produced via direct amination with various amines in moderate to high yields. The formal synthesis of Suvorexant, a medication for the treatment of insomnia, was accomplished using a developed amination process. The reaction was completed in an hour at 100-150 °C in a microwave reactor without the use of external catalyst or additive. Key benefits of this process include an on-water reaction, short reaction time, being scalable and catalyst-free, and use of 2-mercaptobenzoxazoles as an inexpensive starting material having low environmental impact in its preparation.
