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1-(1,3-benzoxazol-2-yl)methanesulfonamide is a chemical compound characterized by the presence of a benzoxazole ring connected to a methanesulfonamide functional group. 1-(1,3-benzoxazol-2-yl)methanesulfonamide exhibits unique optical properties, making it a versatile molecule with potential applications in various industries.

73101-70-9

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73101-70-9 Usage

Uses

Used in the Plastics Industry:
1-(1,3-benzoxazol-2-yl)methanesulfonamide is used as a fluorescent whitening agent for enhancing the brightness and color of plastic products. Its ability to absorb light in the ultraviolet and violet region of the electromagnetic spectrum and re-emit it in the blue region improves the overall appearance of the plastics.
Used in the Textile Industry:
In the textile industry, 1-(1,3-benzoxazol-2-yl)methanesulfonamide serves as a valuable additive to improve the brightness and color of fibers. Its fluorescent properties contribute to the enhancement of the visual appeal of textile products, making them more attractive to consumers.
Used in the Paper Industry:
1-(1,3-benzoxazol-2-yl)methanesulfonamide is also utilized as a fluorescent whitening agent in the paper industry. By absorbing and re-emitting light, it helps to improve the brightness and color of papers, resulting in higher quality and more visually appealing products.
Used in Pharmaceutical Research:
1-(1,3-benzoxazol-2-yl)methanesulfonamide has been studied for its potential biological activity, particularly as an anti-cancer agent. Its ability to inhibit protein-protein interactions makes it a promising candidate for further research and development in the field of oncology.
However, it is important to note that further research is necessary to fully understand the potential applications and effects of 1-(1,3-benzoxazol-2-yl)methanesulfonamide in these industries and areas of study.

Check Digit Verification of cas no

The CAS Registry Mumber 73101-70-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,0 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73101-70:
(7*7)+(6*3)+(5*1)+(4*0)+(3*1)+(2*7)+(1*0)=89
89 % 10 = 9
So 73101-70-9 is a valid CAS Registry Number.

73101-70-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-benzoxazol-2-ylmethanesulfonamide

1.2 Other means of identification

Product number -
Other names 2-Benzoxazolemethanesulfonamide

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:73101-70-9 SDS

73101-70-9Downstream Products

73101-70-9Relevant academic research and scientific papers

Syntheses of 2-sulfamoylmethylbenzoxazole derivatives and determination of their anticonvulsant activities

Uno,Kurokawa,Masuda

, p. 2359 - 2361 (2007/10/02)

Some 2-sulfamoylmethylbenzoxazole derivatives were synthesized from 2-bromomethylbenzoxazole by reaction with sodium bisulfite, followed by chlorination and amination. Among them, 2-sulfamoylmethylbenzoxazole showed the strongest anticonvulsant activity, which was compared with that of 3-sulfamoylmethyl-1,2-benzisoxazole (I).

Methane-sulfonamide derivatives, the preparation thereof and composition comprising the same

-

, (2008/06/13)

Methane-sulfonamide derivatives of the formula: STR1 wherein R1 is hydrogen or a halogen atom, R2 and R3 are the same or different and are each hydrogen or a straight or branched alkyl having 1 to 3 carbon atoms, and one of X and Y is a carbon atom and another is a nitrogen atom, provided that the group: --CH2 SO2 NR2 R3 is bonded to the carbon atom of either of X and Y, and an alkali metal salt thereof, and a process for the preparation of said methane-sulfonamide derivatives. Said compounds have an excellent anticonvulsant activity and are useful as anticonvulsants for controlling convulsions and seizures in patients with epilepsy.

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