77455-54-0

Basic information

• Product Name: (2-chloro-4-nitrophenyl)methanediyl diacetate
• CAS NO: 77455-54-0
• Molecular Formula: C₁₁H₁₀ClNO₆
• Molecular Weight: 287.6532
• Mol File: 77455-54-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 392.9°C at 760 mmHg
• Flash Point: 191.4°C
• Density: 1.415g/cm³
• Vapor Pressure: 2.21E-06mmHg at 25°C
• Refractive Index: 1.549
• CAS DataBase Reference: (2-chloro-4-nitrophenyl)methanediyl diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (2-chloro-4-nitrophenyl)methanediyl diacetate(77455-54-0)
• EPA Substance Registry System: (2-chloro-4-nitrophenyl)methanediyl diacetate(77455-54-0)

Safety Data

• Hazardous Substances Data: 77455-54-0(Hazardous Substances Data)

Usage

Description

(2-chloro-4-nitrophenyl)methanediyl diacetate, also known as 2-chloro-4-nitrophenyl-methanediyl diacetate or 2-chloro-4-nitrophenyl diacetate, is an organic chemical compound with the molecular formula C10H8ClNO6. It is a pale yellow to light brown solid that is sparingly soluble in water. (2-chloro-4-nitrophenyl)methanediyl diacetate is primarily used as an intermediate in the synthesis of other chemicals and pharmaceuticals.

Uses

Used in Chemical Synthesis:
(2-chloro-4-nitrophenyl)methanediyl diacetate is used as an intermediate in the chemical synthesis industry for the production of other organic compounds. Its unique structure allows it to be a versatile building block in the creation of various chemical products.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, (2-chloro-4-nitrophenyl)methanediyl diacetate is used as an intermediate in the manufacturing of pharmaceuticals. Its reactivity and functional groups make it a valuable component in the development of new drugs and medications.
It is important to handle (2-chloro-4-nitrophenyl)methanediyl diacetate with care, as it may be harmful if swallowed, inhaled, or if it comes into contact with the skin. Proper safety measures should be taken during its use and disposal to minimize any potential risks.

Upstream product

• 121-86-8 2-chloro-4-nitrotoluene 
• 108-24-7 acetic anhydride 

Downstream Products

• 5568-33-2 2-chloro-4-nitrobenzaldehyde 
• 198821-76-0 3-chloro-4-(oxazol-5-yl)phenylamine 
• 73097-02-6 ethyl 2-chloro-4-nitrobenzoate 
• 77455-65-3 3-chloro-4-(dichloromethyl)-1-nitrobenzene 
• 77455-68-6 2,2'-dichloro-4,4'-dinitrodiphenylacetylene 
• 77455-66-4 (Z)-α,α',2,2'-tetrachloro-4,4'-dinitrostilbene 
• 77455-67-5 (E)-α,α',2,2'-tetrachloro-4,4'-dinitrostilbene 

Relevant articles and documents

Synthesis, larvicidal activity, and SAR studies of new benzoylphenylureas containing oxime ether and oxime ester group

A series of new structural benzoylphenylureas (BPUs) containing oxime ether and oxime ester group were designed and synthesized. The larvicidal activities against Oriental armyworm and mosquito of these benzoylphenylureas were evaluated and the result of bioassay displayed specific structure-activity relationship (SAR). Most of the compounds exhibited excellent larvicidal activities against Oriental armyworm and mosquito. Interestingly, some compounds showed different structure-activity relationship towards diamondback moth, beet armyworm, and corn borer although three tested insects all belong to the same insect order.

Novel diamide-based inhibitors of IMPDH

A series of novel amide-based small molecule inhibitors of inosine monophosphate dehydrogenase is described. The synthesis and the structure-activity relationships (SARs) derived from in vitro studies are presented.

Organic nonlinear optical material

The present invention provides an organic nonlinear optical material including a benzylidene-aniline derivative having an electron-donating substituent introduced at the 4-position and an electron-accepting substituent introduced at the 4'-position, by se