59776-60-2 Usage
Description
3,5-Dinitrophenyl isocyanate is a highly reactive chemical compound used in organic synthesis and as a building block for the production of various polymers and pharmaceuticals. It is known for its ability to undergo nucleophilic additions and substitutions, making it a versatile reagent in organic chemistry. However, it is a hazardous substance that requires careful handling and storage due to its potential to cause skin and respiratory irritation, as well as its explosive properties.
Uses
Used in Organic Synthesis:
3,5-Dinitrophenyl isocyanate is used as a reagent in organic synthesis for its ability to undergo nucleophilic additions and substitutions, making it a versatile compound in the creation of various organic molecules.
Used in Polymer Production:
3,5-Dinitrophenyl isocyanate is used as a building block in the production of diisocyanates, which are key components in the manufacturing of polyurethane foams, coatings, and adhesives.
Used in Pharmaceutical Production:
3,5-Dinitrophenyl isocyanate is used as a starting material in the synthesis of certain pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Safety and Handling Protocols:
Due to its hazardous nature, 3,5-dinitrophenyl isocyanate is used as a subject for the development and implementation of safety protocols and handling procedures to minimize risks associated with its use, such as skin and respiratory irritation and potential for explosion.
Check Digit Verification of cas no
The CAS Registry Mumber 59776-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,7 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59776-60:
(7*5)+(6*9)+(5*7)+(4*7)+(3*6)+(2*6)+(1*0)=182
182 % 10 = 2
So 59776-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H3N3O5/c11-4-8-5-1-6(9(12)13)3-7(2-5)10(14)15/h1-3H
59776-60-2Relevant articles and documents
[3]rotaxanes composed of two dibenzo-24-crown-8 ether wheels and an azamacrocyclic complex
Wo?ny, Mateusz,Wi?ckowska, Agnieszka,Trzybiński, Damian,Sutu?a, Szymon,Domaga?a, S?awomir,Wo?niak, Krzysztof
, p. 15845 - 15856 (2018/11/23)
The azamacrocyclic complex was used as a platform for the construction of [3]rotaxanes containing two DB24C8 macrocycles per molecule. The complex unit incorporates two electron deficient π-bond systems and two N-H hydrogen bond donating groups which faci
Additions of Chiral Allyltitanocenes to Aldehydes: Diastereoselective Synthesis of Homoallylic Alcohols with a Recyclable Chiral Transition Metal Reagent
Collins, Scott,Kuntz, Bradley A.,Hong, Yaping
, p. 4154 - 4158 (2007/10/02)
Homochiral allyl- and crotyltitanocenes 4a (R = H) and 4b (R = Me) prepared from ansa-titanocene dichloride 2 react with aldehydes to provide on workup homoallylic alcohols 5 in excellent yield and with moderate to excellent anti diastereoselectivity in t
