82475-64-7 Usage
Molecular weight
434.29 g/mol
Appearance
Colorless to pale yellow liquid
Density
1.21 g/cm3
Boiling point
150-160°C (302-320°F) at 1.5 mmHg
Flash point
Not available
Solubility
Soluble in organic solvents such as ethanol, methanol, and acetone
Reactivity
Used as a reactive diluent in the production of polymer materials and as a crosslinking agent in the synthesis of silicone-based polymers
Applications
Commonly used in the manufacturing of adhesives, sealants, and coatings, as well as in the formulation of personal care products and pharmaceuticals
Derivative
A derivative of 1,3-bis(2-chloroethyl)-1-nitrosourea, a cancer-treating agent
Health hazards
Potential skin and eye irritation, respiratory problems, and potential carcinogenic effects
Safety measures
Careful handling and appropriate safety measures are necessary when working with this chemical compound to avoid risks to human health and the environment
Please note that some specific content, such as the flash point, may not be available or well-documented in the provided material.
Check Digit Verification of cas no
The CAS Registry Mumber 82475-64-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,4,7 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82475-64:
(7*8)+(6*2)+(5*4)+(4*7)+(3*5)+(2*6)+(1*4)=147
147 % 10 = 7
So 82475-64-7 is a valid CAS Registry Number.
82475-64-7Relevant academic research and scientific papers
Synthesis, hydrolytic reactivity, and anticancer evaluation of N-and O-triorganosilylated compounds as new types of potential prodrugs
Chiu,Chang,Ozkan,Zon,Fichter,Phillips
, p. 542 - 551 (2007/10/02)
N- and O-Triorganosilylated compounds related to various anticancer agents were synthesized for evaluation as potential anticancer prodrugs. 1H-NMR and UV kinetic measurements of hydrolytic desilylation were used to correlate relative rates of structural unmasking with steric bulk about the silicon reaction center. The tert-butyldimethylsilyl ester of chlorambucil and a number of O-triorganosilylated carbamate derivatives of nor-nitrogen mustard showed significant activity against P-388 lymphocytic leukemia in mice.
