13533-12-5

Basic information

• Product Name: (E)-1-chloro-1-{(4E)-4-[chloro(nitroso)methylidene]cyclohexa-2,5-dien-1-ylidene}-N-hydroxymethanamine
• CAS NO: 13533-12-5
• Molecular Formula: C₈H₆Cl₂N₂O₂
• Molecular Weight: 233.0514
• Mol File: 13533-12-5.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 230.4°C at 760 mmHg
• Flash Point: 93.2°C
• Density: 1.49g/cm³
• Vapor Pressure: 0.0125mmHg at 25°C
• Refractive Index: 1.609
• CAS DataBase Reference: (E)-1-chloro-1-{(4E)-4-[chloro(nitroso)methylidene]cyclohexa-2,5-dien-1-ylidene}-N-hydroxymethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-chloro-1-{(4E)-4-[chloro(nitroso)methylidene]cyclohexa-2,5-dien-1-ylidene}-N-hydroxymethanamine(13533-12-5)
• EPA Substance Registry System: (E)-1-chloro-1-{(4E)-4-[chloro(nitroso)methylidene]cyclohexa-2,5-dien-1-ylidene}-N-hydroxymethanamine(13533-12-5)

Safety Data

• Hazardous Substances Data: 13533-12-5(Hazardous Substances Data)

Usage

General Description

(E)-1-chloro-1-{(4E)-4-[chloro(nitroso)methylidene]cyclohexa-2,5-dien-1-ylidene}-N-hydroxymethanamine, also known as nitrosochloromethane, is a chemical compound with the molecular formula C7H8Cl2NO. It is a highly reactive, colorless liquid with a pungent odor, and it is primarily used in organic synthesis for the production of various chemical compounds. Nitrosochloromethane is classified as a chloroalkene and a nitro compound, and it is considered to be a potentially hazardous chemical due to its toxicity and reactivity. It should be handled with care, and its use should be strictly regulated to prevent harm to human health and the environment.

Upstream product

• 623-27-8 terephthalaldehyde, 
• 69386-99-8 terephthalaldehyde oxime 

Downstream Products

• 1047-63-8 1,4-bis-(2-benzimidazolyl)benzene 
• 3729-34-8 terephthalobis(nitrile N-oxide) 
• 1402043-67-7 1,4-bis-(4,5-dihydro-5-isoxazolecarbonitrie-3-yl)benzene 
• 1402043-64-4 1,4-bis-(4,5-dihydro-5-isoxazol-3-yl ethyl ether)benzene 
• 3729-06-4 1,4-bis-(5-phenyl-4,5-dihydroxazole-3-yl)benzene 
• 1204591-34-3 1,4-bis(4-nitrofuroxan-3-yl)benzene 
• 1204591-31-0 1,4-bis(3-nitrofuroxan-4-yl)benzene 
• 195394-94-6 1,4-bis(cyanooximinomethyl)benzene 
• 287398-43-0 C₂₄H₄₀N₂O₄Si₄ 
• 20155-72-0 octa-N-ethyl-4,5,4',5'-tetrahydro-3,3'-p-phenylene-bis-isoxazole-4,5-diamine 

Relevant articles and documents

One-pot synthesis of precise polyisoxazoles by click polymerization: Copper (I)-catalyzed 1,3-dipolar cycloaddition of nitrile oxides with alkynes

This article reports a new one-pot method for polymer preparation, which involves double click chemistry. In one pot, two click reactions take place sequentially by adding the reactants step by step. The first click reaction is to produce the monomer for

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The 1,3- and 1,4-bis(3-nitrofurazan-4-yl)benzenes have been synthesized by dehydration of 1,3- and 1,4-bis(2-aminoglyoximo- 1-yl)benzenes followed by oxidation of amino groups. The 1,3- and 1,4-bis(3-nitrofuroxan-4-yl)benzenes have been prepared by nitroz

Crown Ether-Type Cyclophanes: Efficient Synthesis via Quadruple or Double Cycloadditions and Molecular Recognition Study

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