14435-21-3 Usage
Type of compound
Diol
Structure
Two hydroxyl groups (-OH) attached to adjacent carbon atoms
Usage
Building block in the synthesis of polymers and other chemical compounds
Industrial applications
Production of polyester resins, polyurethanes, and surfactants
Additional use
Monomer in the production of water-soluble and biodegradable polymers
Physical state
White, crystalline solid at room temperature
Stability
Relatively stable under normal conditions
Toxicity
Low-toxicity compound
Health concerns
No significant health concerns associated with its use in industrial settings
Check Digit Verification of cas no
The CAS Registry Mumber 14435-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,3 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14435-21:
(7*1)+(6*4)+(5*4)+(4*3)+(3*5)+(2*2)+(1*1)=83
83 % 10 = 3
So 14435-21-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H24O2/c13-11-7-3-1-2-4-8-12(14)10-6-5-9-11/h11-14H,1-10H2
14435-21-3Relevant articles and documents
Microbiological hydroxylation. 8. Cyclododecanone and cyclopentadecanone as substrates for steroid-hydroxylating fungi.
Ashton,Bailey,Jones
, p. 1665 - 1669 (1974)
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Selective biocatalytic hydroxylation of unactivated methylene C-H bonds in cyclic alkyl substrates
Sarkar, Md Raihan,Dasgupta, Samrat,Pyke, Simon M.,Bell, Stephen G.
supporting information, p. 5029 - 5032 (2019/05/21)
The cytochrome P450 monooxygenase CYP101B1 from Novosphingobium aromaticivorans selectively hydroxylated methylene C-H bonds in cycloalkyl rings. Cycloketones and cycloalkyl esters containing C6, C8, C10 and C12 rings were oxidised with high selectively on the opposite side of the ring to the carbonyl substituent. Cyclodecanone was oxidised to oxabicycloundecanol derivatives in equilibrium with the hydroxycyclodecanones.
