30485-71-3 Usage
Description
1-CHLORO-4-HYDROXYCYCLOHEXANE, also known as 4-chlorocyclohexanol, is an organic compound with a chloro substituent at the first carbon and a hydroxyl group at the fourth carbon of the cyclohexane ring. It is a colorless liquid with a mild, sweet odor and is soluble in water and various organic solvents. 1-CHLORO-4-HYDROXYCYCLOHEXANE is known for its chemical reactivity and is used as an intermediate in the synthesis of various chemicals and pharmaceuticals.
Uses
Used in Chemical Synthesis:
1-CHLORO-4-HYDROXYCYCLOHEXANE is used as a chemical intermediate for the production of various chemicals and pharmaceuticals. Its unique structure allows for further functionalization and modification, making it a versatile building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
1-CHLORO-4-HYDROXYCYCLOHEXANE is used as a starting material for the synthesis of various pharmaceutical compounds. Its reactivity and structural features make it a valuable component in the development of new drugs and therapeutic agents.
Used in Environmental Applications:
1-CHLORO-4-HYDROXYCYCLOHEXANE is used as a carbon source to identify specific microorganisms, such as Acidovorax CHX100 and Chelatococcus CHX1100, from soil samples. This application aids in the study of microbial diversity and the role of these microorganisms in environmental processes.
Check Digit Verification of cas no
The CAS Registry Mumber 30485-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,4,8 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30485-71:
(7*3)+(6*0)+(5*4)+(4*8)+(3*5)+(2*7)+(1*1)=103
103 % 10 = 3
So 30485-71-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H11ClO/c7-5-1-3-6(8)4-2-5/h5-6,8H,1-4H2
30485-71-3Relevant articles and documents
An efficient route to alkyl chlorides from alcohols using the complex TCT/DMF
De Luca, Lidia,Giacomelli, Giampaolo,Porcheddu, Andrea
, p. 553 - 555 (2007/10/03)
(formula presented) Efficient conversion of alcohols and β-amino alcohols to the corresponding chlorides (and bromides) can be carried out at room temperature in methylene chloride, using 2,4,6-trichloro[1,3,5]triazine and N,N-dimethyl formamide. This procedure can also be applied to optically active carbinols.