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Methanesulfonamide, N-(2-hydroxyphenyl)-, also known as 2-(Methanesulfonamido)phenol, is an organic chemical compound that serves as a pharmaceutical intermediate in the synthesis of various medications. It belongs to the sulfonamide class of compounds, which are recognized for their antibacterial and antifungal properties. The unique feature of Methanesulfonamide,N-(2-hydroxyphenyl)- is the hydroxyphenyl group attached to the nitrogen atom, which endows it with potential antioxidant and anti-inflammatory properties. This makes it a versatile compound for use in the development of drugs targeting a range of conditions.

6912-38-5

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6912-38-5 Usage

Uses

Used in Pharmaceutical Industry:
Methanesulfonamide, N-(2-hydroxyphenyl)is used as a pharmaceutical intermediate for the synthesis of medications that treat a variety of conditions. Its antibacterial and antifungal properties make it suitable for the development of drugs to combat microbial infections.
Used in Anti-inflammatory and Antioxidant Applications:
Due to its hydroxyphenyl group, Methanesulfonamide, N-(2-hydroxyphenyl)is used as an anti-inflammatory and antioxidant agent in the formulation of drugs. This dual functionality can be beneficial in the treatment of conditions such as arthritis, where both inflammation and oxidative stress play a role in the disease progression.
Used in Anticancer Drug Development:
Methanesulfonamide, N-(2-hydroxyphenyl)is used as a component in the development of anticancer drugs. Its potential antioxidant properties may contribute to reducing oxidative stress associated with cancer, and its anti-inflammatory effects could help manage inflammation related to cancer progression.
Used in Cosmetic and Personal Care Industry:
Methanesulfonamide, N-(2-hydroxyphenyl)is used as a skin conditioning agent and for its anti-aging effects in cosmetic and personal care products. Its antioxidant properties may help protect the skin from oxidative damage, while its anti-inflammatory effects could soothe and reduce inflammation in the skin, contributing to a more youthful appearance.

Check Digit Verification of cas no

The CAS Registry Mumber 6912-38-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,1 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6912-38:
(6*6)+(5*9)+(4*1)+(3*2)+(2*3)+(1*8)=105
105 % 10 = 5
So 6912-38-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO3S/c1-12(10,11)8-6-4-2-3-5-7(6)9/h2-5,8-9H,1H3

6912-38-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-hydroxyphenyl)methanesulfonamide

1.2 Other means of identification

Product number -
Other names Methanesulfonanilide,2'-hydroxy

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:6912-38-5 SDS

6912-38-5Relevant academic research and scientific papers

NOVEL COMPOUNDS

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Page/Page column 39; 40, (2018/04/12)

The present invention provides compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein n, X1, X2, R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, R12and R13 are as defined in the specification, processes for their preparation, pharmaceutical compositions containing them and their use in therapy.

Use of 2-(sulphonylamino) phenols as couplers in oxidation colouring

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, (2008/06/13)

The invention relates to the field of the oxidation dyeing of keratinous fibres and in particular of human keratinous fibers, such as the hair. The invention relates more particularly to the use of certain 2-(sulphonylamino)phenols of following formula (I) as coupler in combination with oxidation dye precursors for 1the oxidation dyeing of the fibers.

1,3,2λ5-Benzothiazaphosphole 2-Oxide and 1,3,2λ5-Benzoxazaphosphole 2-Oxide Derivatives, New and Versatile Phosphorylating Reagents

Jacob, Peter,Richter, Wolfgang,Ugi, Ivar

, p. 519 - 522 (2007/10/02)

The synthesis of the highly reactive five-membered cyclic phosphorylating reagents 6a and 12 is decribed.The reagent 6a monophosphorylates alcohols without ring opening, whereas 12 diphosphorylates with ring opening yielding phosphate triesters.

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