189572-01-8 Usage
Chemical structure
1,3-Propanediol, 2-(4-nitrophenyl)-, dinitrate (ester) is a chemical compound with a 1,3-propanediol backbone and a nitrate ester group attached to a 4-nitrophenyl group.
Functional groups
The compound contains a nitrate ester group, a 1,3-propanediol backbone, and a 4-nitrophenyl group.
Applications
It is commonly used in the production of explosives and propellants due to its explosive properties.
Reactivity
1,3-Propanediol, 2-(4-nitrophenyl)-, dinitrate (ester) is highly reactive and should be handled with caution.
Safety protocols
It is important to follow proper safety protocols when working with 1,3-Propanediol, 2-(4-nitrophenyl)-, dinitrate (ester) to prevent accidents or chemical reactions.
Physical state
The compound is likely a solid at room temperature, as many nitrate esters are solids.
Sensitivity
Due to its explosive properties, 1,3-Propanediol, 2-(4-nitrophenyl)-, dinitrate (ester) is sensitive to heat, impact, and friction.
Stability
The compound may be sensitive to decomposition or degradation under certain conditions, such as high temperatures or exposure to light.
Hazards
In addition to its explosive properties, 1,3-Propanediol, 2-(4-nitrophenyl)-, dinitrate (ester) may pose other hazards, such as toxicity or environmental concerns.
Storage and handling
The compound should be stored in a cool, dry, and well-ventilated area, away from heat sources, sparks, and open flames. It should be handled using appropriate personal protective equipment (PPE) and in accordance with relevant safety guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 189572-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,5,7 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 189572-01:
(8*1)+(7*8)+(6*9)+(5*5)+(4*7)+(3*2)+(2*0)+(1*1)=178
178 % 10 = 8
So 189572-01-8 is a valid CAS Registry Number.
189572-01-8Relevant articles and documents
Reactions of 3-phenyloxetane and 7-oxabicyclo[2.2.1]heptane with dinitrogen pentoxide in dichloromethane
Dormer, Jonathan C.,Hylands, Kevin A.,Moodie, Roy B.
, p. 243 - 246 (1998)
3-Phenyloxetane reacts initially almost entirely by ortho and para aromatic nitration. This is followed by oxetane ring-opening to give the corresponding 2-arylpropane-1,3-diol dinitrates. The oxetane ring-opening reactions, and the reaction of 7-oxabicyc
Design and synthesis of benzoic acid derivatives as influenza neuraminidase inhibitors using structure-based drug design
Chand, Pooran,Babu, Yarlagadda S.,Bantia, Shanta,Chu, Naiming,Cole, L. Brent,Kotian, Pravin L.,Laver, W. Graeme,Montgomery, John A.,Pathak, Ved P.,Petty, Sandra L.,Shrout, David P.,Walsh, David A.,Walsh, Gerald M.
, p. 4030 - 4052 (2007/10/03)
A series of 94 benzoic acid derivatives was synthesized and tested for its ability to inhibit influenza neuraminidase. The enzyme-inhibitor complex structure was determined by X-ray crystallographic analysis for compounds which inhibited the enzyme. The most potent compound tested in vitro, 5 (4- (acetylamino)-3-guanidinobenzoic acid), had an IC50 = 2.5 x 10-6 M against N9 neuraminidase. Compound 5 was oriented in the active site of the neuraminidase in a manner that was not predicted from the reported active site binding of GANA (4) with neuraminidase. In a mouse model of influenza, 5 did not protect the mice from weight loss due to the influenza virus when dosed intranasally.
