60901-05-5 Usage
Synonyms
cis-cyclohexanedicarbonyl dichloride
Physical state
Colorless liquid
Solubility
Insoluble in water, soluble in organic solvents
Primary uses
Production of plastics, polymers, and other industrial materials
Role in synthesis
Key intermediate in the synthesis of various organic compounds
Application as a reagent
Used in chemical reactions
Industrial applications
Crosslinking polymers and modifying their physical and chemical properties
Safety concerns
Toxic and a potential irritant to the skin and respiratory system
Handling precautions
Handle with caution due to its toxic nature and potential for irritation
Check Digit Verification of cas no
The CAS Registry Mumber 60901-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,0 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60901-05:
(7*6)+(6*0)+(5*9)+(4*0)+(3*1)+(2*0)+(1*5)=95
95 % 10 = 5
So 60901-05-5 is a valid CAS Registry Number.
60901-05-5Relevant articles and documents
Rational tuning chelate size of bis-oxazoline ligands to improve enantioselectivity in the asymmetric aziridination of chalcones
Ma, Linge,Du, Da-Ming,Xu, Jiaxi
, p. 10155 - 10158 (2007/10/03)
Chalcones were asymmetrically aziridinated with [N-(p-toluenesulfonyl) imino]phenyliodinane (PhI=NTs) as a nitrene source under catalysis of CuOTf and a series of cyclohexane-linked bis-oxazolines (cHBOXes), which are chelate size rationally tuned bis-oxazolines. The results indicate that highly enantioselective aziridination of chalcones with up to >99% ee have been achieved under catalysis of (S,S)-1,2-bis[(S)-(4-phenyl)oxazolin-2-yl] cyclohexane, which is the most-matched stereoisomer among cyclohexane-linked bis-oxazolines. It was also found that the enantioselectivity is not substituent-dependent with respect to chalcones in the present case, unlike with 1,8-anthracene-linked bis-oxazolines (AnBOXes).
