40861-08-3 Usage
Description
N,N-Di(4-chlorobenzyl)hydroxylamine is a water-soluble, crystalline solid that is used as a reagent and intermediate in the pharmaceutical and agricultural industries for the synthesis of various products. It has the ability to form bonds with organic compounds, making it useful in the preparation of diverse chemical compounds. Additionally, it exhibits antioxidant and anti-inflammatory properties, making it potentially useful for medical and cosmetic applications. However, it is important to handle this compound with care, as it can be harmful if ingested or inhaled, and can cause irritation to the skin and eyes.
Uses
Used in Pharmaceutical Industry:
N,N-Di(4-chlorobenzyl)hydroxylamine is used as a reagent and intermediate for the synthesis of various pharmaceutical products. Its ability to form bonds with organic compounds makes it useful in the preparation of diverse chemical compounds.
Used in Agricultural Industry:
N,N-Di(4-chlorobenzyl)hydroxylamine is used as a reagent and intermediate for the synthesis of various agricultural products. Its ability to form bonds with organic compounds makes it useful in the preparation of diverse chemical compounds.
Used in Medical Applications:
N,N-Di(4-chlorobenzyl)hydroxylamine is used as an antioxidant and anti-inflammatory agent due to its potential medical benefits.
Used in Cosmetic Applications:
N,N-Di(4-chlorobenzyl)hydroxylamine is used as an antioxidant and anti-inflammatory agent in cosmetic products due to its potential benefits for skin health.
Check Digit Verification of cas no
The CAS Registry Mumber 40861-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,6 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40861-08:
(7*4)+(6*0)+(5*8)+(4*6)+(3*1)+(2*0)+(1*8)=103
103 % 10 = 3
So 40861-08-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H13Cl2NO/c15-13-5-1-11(2-6-13)9-17(18)10-12-3-7-14(16)8-4-12/h1-8,18H,9-10H2
40861-08-3Relevant articles and documents
The Reactivity of Difluorocarbene with Hydroxylamines: Synthesis of Carbamoyl Fluorides
Baars, Hannah,Engel, Julien,Mertens, Lucas,Meister, Daniela,Bolm, Carsten
supporting information, p. 2293 - 2299 (2016/07/29)
Carbamoyl fluorides are formed in reactions of hydroxylamines with difluorocarbene generated from sodium bromodifluoroacetate as readily available and non-toxic carbene precursor. The process shows a high functional group tolerance, and the reaction path has been rationalized by computational calculations. (Figure presented.) .
Mechanism of the 10-methylacridinium ion-sensitized photooxidation of N,N-dibenzylhydroxylamine and its derivatives in acetonitrile
Ohba, Yasuhiro,Kubo, Kanji,Igarashi, Tetsutaro,Sakurai, Tadamitsu
, p. 491 - 493 (2007/10/03)
The 10-methylacridinium ion (MA+)-sensitized photooxidation of substituted N,N-dibenzylhydroxylamines (1) in acetonitrile occurred mainly by a superoxide ion mechanism to give N-benzylidenebenzylamine N-oxides (2) and hydrogen peroxide quantitatively. Analysis of substituent effects on the limiting quantum yield for formation of 2 showed that back electron transfer (ET) from the 10-methylacridinyl radical (MA.) to the radical cation 1+. proceeds in the Marcus 'normal region'. In addition, this back ET was found to take place in preference to one-electron reduction of O2 by MA..
