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Hydroxylamine, O-(3-chlorophenyl)-, hydrochloride is a chemical compound with the formula C6H7Cl2NO. It is a derivative of hydroxylamine, where a 3-chlorophenyl group is attached to the hydroxylamine molecule, and a hydrochloride ion is present. Hydroxylamine, O-(3-chlorophenyl)-, hydrochloride is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and other chemicals. It is a white crystalline solid that is soluble in water and has a melting point of approximately 195-200°C. Due to its reactivity, it is important to handle Hydroxylamine, O-(3-chlorophenyl)-, hydrochloride with care, as it can be toxic and may cause irritation to the skin, eyes, and respiratory system.

4107-36-2

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4107-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4107-36-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,0 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4107-36:
(6*4)+(5*1)+(4*0)+(3*7)+(2*3)+(1*6)=62
62 % 10 = 2
So 4107-36-2 is a valid CAS Registry Number.

4107-36-2Relevant academic research and scientific papers

NOVEL VASCULAR LEAKAGEAGE INHIBITOR

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Paragraph 0132, (2015/01/07)

The present disclosure relates to a novel vascular leakage inhibitor. The novel vascular leakage inhibitor of the present invention inhibits the apoptosis of vascular endothelial cells, inhibits the formation of actin stress fibers induced by VEGF, and enhances the cortical actin ring structure, thereby inhibiting vascular leakage. Accordingly, the vascular leakage inhibitor of the present invention can prevent or treat various diseases caused by vascular leakage. Since the vascular leakage inhibitor of the present invention is synthesized from commercially available or easily synthesizable pregnenolones, it has remarkably superior feasibility of commercial synthesis.

Nucleophilic Aromatic Substitution on Tricarbonyl(halogenoarene)chromium Complexes: A New Synthesis of O-Arylhydroxylamines

Baldoli, Clara,Buttero, Paola Del,Licandro, Emanuela,Maiorana, Stefano

, p. 344 - 345 (2007/10/02)

A series of O-arylhydroxylamines 4 have been synthesized under mild conditions and in good yields by the reaction of tricarbonyl(halogenoarene)chromium complexes 1 with N-(tert-butyloxycarbonyl)hydroxylamine (tert-butyl N-hydroxycarbamate), followed by decomplexation and acidic hydrolysis of the tert-butyl N-(aryloxy)carbamates 3.

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