1203-55-0 Usage
Description
NAPHTHO[2,1-D]THIAZOL-2-YLAMINE is a heterocyclic organic compound characterized by the presence of a thiazol and naphthalene ring fused together. It features an amine functional group attached to the thiazole ring, which contributes to its chemical reactivity and potential applications in various fields.
Uses
Used in Organic Synthesis:
NAPHTHO[2,1-D]THIAZOL-2-YLAMINE is used as a key intermediate in the synthesis of various heterocyclic compounds, which are valuable building blocks for the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
NAPHTHO[2,1-D]THIAZOL-2-YLAMINE is used as a starting material for the development of novel therapeutic agents, particularly those targeting specific biological pathways or receptors. Its unique structure and reactivity make it a promising candidate for the design of new drugs with improved efficacy and selectivity.
Used in OLED Industry:
NAPHTHO[2,1-D]THIAZOL-2-YLAMINE is used as a precursor in the preparation of heteroaryl compounds, which are essential components in the fabrication of organic light-emitting diodes (OLEDs). These compounds contribute to the efficient emission of light and improved device performance in OLED applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1203-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1203-55:
(6*1)+(5*2)+(4*0)+(3*3)+(2*5)+(1*5)=40
40 % 10 = 0
So 1203-55-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H8N2S/c12-11-13-9-6-5-7-3-1-2-4-8(7)10(9)14-11/h1-6H,(H2,12,13)
1203-55-0Relevant articles and documents
Visible-light-initiated malic acid-promoted cascade coupling/cyclization of aromatic amines and KSCN to 2-aminobenzothiazoles without photocatalyst
He, Wei-Bao,Gao, Lan-Qing,Chen, Xin-Jie,Wu, Zhi-Lin,Huang, Ying,Cao, Zhong,Xu, Xin-Hua,He, Wei-Min
, p. 1895 - 1898 (2020)
By using ambient air as the oxidant and malic acid as the promoter, a practical method for the preparation of 2-aminobenzothiazoles through visible-light-initiated cascade reaction of aromatic amines and KSCN in eco-friendly bis(methoxypropy)ether under metal-, hazardous additive-, photocatalyst-free conditions was established.
NAPHTHO[2,1 -D]THIAZOLE DERIVATIVES, COMPOSITIONS THEREOF AND METHODS OF TREATING DISORDERS
-
Paragraph 0065, (2021/05/29)
The present application relates to the compounds of formula (I) that inhibit CDK9, pharmaceutical compositions thereof and methods of making and using the same.
Metal-free synthesis of 2-aminobenzothiazoles via aerobic oxidative cyclization/dehydrogenation of cyclohexanones and thioureas
Zhao, Jinwu,Huang, Huawen,Wu, Wanqing,Chen, Huoji,Jiang, Huanfeng
supporting information, p. 2604 - 2607 (2013/07/11)
A metal-free process for the synthesis of 2-aminobenzothiazoles from cyclohexanones and thioureas has been developed using catalytic iodine and molecular oxygen as the oxidant under mild conditions. Various 2-aminobenzothiazoles, 2-aminonaphtho[2,1-d]thiazoles, and 2-aminonaphtho[1,2-d] thiazoles were prepared via this method in satisfactory yields.