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N-(4-hydroxyphenyl)-N-methyl-nitrous amide, also known as 4-hydroxyphenylmethylnitrosamine or HPMN, is an organic compound with the chemical formula C7H8N2O. It is a derivative of nitrous amide, characterized by the presence of a nitroso group (-N=O) and a hydroxyphenyl group. N-(4-hydroxyphenyl)-N-methyl-nitrous amide is of interest in chemical research due to its potential applications and properties. It is important to note that many nitroso compounds, including HPMN, can be toxic and may have implications for human health and safety, thus requiring careful handling and study. The compound's structure and reactivity make it a subject of interest in the field of organic chemistry, particularly in the study of nitroso compounds and their reactions.

2976-94-5

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2976-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2976-94-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2976-94:
(6*2)+(5*9)+(4*7)+(3*6)+(2*9)+(1*4)=125
125 % 10 = 5
So 2976-94-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2/c1-9(8-11)6-2-4-7(10)5-3-6/h2-5,10H,1H3

2976-94-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-hydroxyphenyl)-N-methylnitrous amide

1.2 Other means of identification

Product number -
Other names N-nitroso-N-methyl-p-hydroxyaniline

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:2976-94-5 SDS

2976-94-5Relevant academic research and scientific papers

Photocontrollable peroxynitrite generator based on N-methyl-N- nitrosoaminophenol for cellular application

Ieda, Naoya,Nakagawa, Hidehiko,Peng, Tao,Yang, Dan,Suzuki, Takayoshi,Miyata, Naoki

supporting information; experimental part, p. 2563 - 2568 (2012/03/22)

We designed and synthesized a photocontrollable peroxynitrite (ONOO -) generator, P-NAP, which has N-methyl-N-nitrosoaminophenol structure with four methyl groups introduced onto the benzene ring to block reaction of the photodecomposition prod

Peptidyl N-nitrosoanilines: A novel class of cysteine protease inactivators

Guo, Zhengmao,Ramirez, Johnny,Li, Jun,Wang, Peng George

, p. 3726 - 3734 (2007/10/03)

A series of peptidyl N-nitrosoanilines were designed, synthesized, and evaluated as inactivators of cysteine protease papain and serine protease chymotrypsin. These new compounds exhibited different inhibitory activities toward the cysteine protease papain in a time- and concentration-dependent manner with second-order rate constants (κ(inact)/K1) ranging over 2 orders of magnitude from 0.604 M-1 s-1 (1) to 100.36 M-1 s-1 (7). No inactivation was observed for serine protease chymotrypsin. Formation of the S-NO bond in papain is supported by several lines of evidences from both spectroscopic studies and chemical analyses. The pH profile more insight into the mechanism of the inactivation process. The covalent yet recoverable cysteine protease inactivation process offers mechanistic implications and endows this new family of inactivators with special properties that are suitable for the development of stable and potent cysteine protease inhibitors.

1-(Arylamino)-and 1-(arylimino)-pyrroles

-

, (2008/06/13)

1-(Arylamino)pyrroles and 1-(arylimino)pyrroles, useful as antibacterial agents, are prepared by reaction of an arylhydrazine or arylhydrazone with a 2,5-di-lower-alkoxytetrahydrofuran or with an alkanedione; by reaction of a 1-arylaminopyrrole with an ox

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