1161009-87-5 Usage
Cyclohexanol derivative
The compound is derived from cyclohexanol, which is a six-carbon ring structure with an alcohol (OH) group attached.
Amino group
The compound contains an amino group (-NH2), which is a common functional group in many pharmaceutical compounds and is known for its ability to form hydrogen bonds and coordinate with other molecules.
Pharmaceutical research use
2-((2-Methoxyethyl)amino)cyclohexanol is used as an intermediate in the synthesis of various drugs and pharmacologically active compounds.
Targeting specific biological pathways
The compound's structure and properties make it useful for creating medications that target specific biological pathways and cellular processes, potentially leading to more effective treatments.
Potential applications in new therapeutic agents
The compound may be used in the development of new therapeutic agents, offering new ways to treat diseases and conditions.
Drug delivery systems
2-((2-Methoxyethyl)amino)cyclohexanol may also have applications in the development of drug delivery systems, which could improve the efficacy and safety of medications.
Check Digit Verification of cas no
The CAS Registry Mumber 1161009-87-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,1,0,0 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1161009-87:
(9*1)+(8*1)+(7*6)+(6*1)+(5*0)+(4*0)+(3*9)+(2*8)+(1*7)=115
115 % 10 = 5
So 1161009-87-5 is a valid CAS Registry Number.
1161009-87-5Relevant articles and documents
A new class of nitrosoureas. VIII. Synthesis and antitumor activity of 3-substituted 1-(2-chloroethyl)-3-(trans-2-hydroxy-cyclohexyl)-1-nitrosoureas
Morikawa,Tsujihara,Takeda,Arai
, p. 1646 - 1651 (2007/10/02)
A series of six 3-substituted 1-(2-chloroethyl)-3-(trans-2-hydroxycyclohexyl)-1-nitrosoureas (IVa-f) was prepared and tested for antitumor activities. Heating of cyclohexene oxide with various alkylamines followed by reaction with 2-chloroethyl isocyanate
