41330-23-8 Usage
General Description
1,2-Cyclopentanediamine, also known as 1,2-diaminocyclopentane or cadaverine, is a chemical compound with the formula C5H12N2. It is a colorless liquid with a distinct odor that is similar to that of rotting flesh. 1,2-Cyclopentanediamine is commonly used in the synthesis of various organic compounds and polymers, and it is also found in certain food products and biological fluids. Due to its foul odor, it is sometimes used as a chemical repellent to deter animals and insects. In high concentrations, 1,2-Cyclopentanediamine can be toxic and may cause irritation to the skin, eyes, and respiratory system.
Check Digit Verification of cas no
The CAS Registry Mumber 41330-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,3 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41330-23:
(7*4)+(6*1)+(5*3)+(4*3)+(3*0)+(2*2)+(1*3)=68
68 % 10 = 8
So 41330-23-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N2/c6-4-2-1-3-5(4)7/h4-5H,1-3,6-7H2
41330-23-8Relevant articles and documents
Paulic et al.
, p. 3463,3464 (1971)
PLATINUM COMPOUND OF MALONIC ACID DERIVATIVE HAVING LEAVING GROUP CONTAINING AMINO OR ALKYLAMINO
-
, (2015/11/16)
Disclosed are a class of platinum compounds of malonic acid derivatives having a leaving group containing an amino or alkylamino, and pharmaceutically acceptable salt thereof, preparation method thereof and pharmaceutical composition containing the compou
The synthesis and use in asymmetric epoxidation of metal salen complexes derived from enantiopure trans-cyclopentane- and cyclobutane-1,2-diamine
Daly, Adrian M.,Gilheany, Declan G.
, p. 127 - 137 (2007/10/03)
A complete synthesis of enantiopure trans-cyclopentane-1,2-diamine and trans-cyclobutane-1,2-diamine is described. These diamines have been used as components of novel chiral salen ligands whose chromium and manganese complexes were then evaluated as oxygen transfer agents in the asymmetric epoxidation of alkenes.
