1379225-92-9 Usage
Uses
Used in Agricultural Industry:
Tert-butyl (3-cyanopropyl)(methyl)carbamate is used as a pesticide or herbicide for its ability to inhibit the growth of unwanted plants or pests. Its selective toxicity ensures that it targets specific organisms while posing minimal harm to others, which is crucial for effective crop protection.
Used in Chemical Processes:
Due to its structural properties and reactivity, tert-butyl (3-cyanopropyl)(methyl)carbamate may also have applications in pharmaceuticals or other chemical processes. Its unique chemical characteristics can be leveraged to develop new compounds or enhance existing processes.
Used in Environmental Management:
Tert-butyl (3-cyanopropyl)(methyl)carbamate is used in controlled doses and formulations to maximize efficacy and minimize environmental impact. Proper handling and disposal procedures are essential to prevent environmental contamination and ensure safety in its use, highlighting its role in responsible environmental management.
Check Digit Verification of cas no
The CAS Registry Mumber 1379225-92-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,2,2 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1379225-92:
(9*1)+(8*3)+(7*7)+(6*9)+(5*2)+(4*2)+(3*5)+(2*9)+(1*2)=189
189 % 10 = 9
So 1379225-92-9 is a valid CAS Registry Number.
1379225-92-9Relevant articles and documents
Electrochemical Tandem Olefination and Hydrogenation Reaction with Ammonia
Zhang, Xiaofeng,Jiang, Runze,Cheng, Xu
, p. 16016 - 16025 (2021/08/24)
An electrochemical Horner-Wadsworth-Emmons/hydrogenation tandem reaction was achieved using ammonia as electron and proton donors. The reaction could give two-carbon-elongated ester and nitrile from aldehyde or ketones directly. This reaction could proceed with a catalytic amount of base or even without a base. The ammonia provides both the electron and proton for this tandem reaction and enables the catalyst-free hydrogenation of an α,β-unsaturated HWE intermediate. More than 40 examples were reported, and functional groups, including heterocycles and hydroxyl, were tolerated.
