503-07-1 Usage
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), and oxygen (O) atoms in the compound.
2. Derivative of undec-9-enoic acid
Explanation
It is derived from undec-9-enoic acid, which is a long-chain fatty acid.
3. Contains a pentyloxiran-2-yl group
Explanation
The compound has a five-membered cyclic ether with a pentyloxy side chain.
Explanation
The stereochemistry of the compound is defined by the (2R,3S) configuration, which refers to the spatial arrangement of atoms around the chiral centers.
Explanation
Due to its unique structure and potential biological activity, the compound may have applications in these industries.
Explanation
The compound is a derivative of a long-chain fatty acid, with an additional cyclic ether side chain attached.
Explanation
The compound has two chiral centers, which are carbon atoms with (2R,3S) configuration.
Stereochemistry
(2R,3S)
Potential applications
Pharmaceutical or chemical industries
Biological activity
Not well studied
Structure
Long-chain fatty acid derivative with a cyclic ether side chain
Number of carbon atoms
20
Number of oxygen atoms
4
Number of hydrogen atoms
34
Chiral centers
2
Check Digit Verification of cas no
The CAS Registry Mumber 503-07-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 503-07:
(5*5)+(4*0)+(3*3)+(2*0)+(1*7)=41
41 % 10 = 1
So 503-07-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H32O3/c1-2-3-10-13-16-17(21-16)14-11-8-6-4-5-7-9-12-15-18(19)20/h8,11,16-17H,2-7,9-10,12-15H2,1H3,(H,19,20)/b11-8-/t16-,17+/m1/s1
503-07-1Relevant articles and documents
Practical, enantiospecific syntheses of 14,15-EET and leukotoxin B (vernolic acid)
Falck,Reddy,Haines, Donovan C.,Reddy, Komandla Malla,Krishna,Graham, Sandra,Murry, Barbara,Peterson, Julian A.
, p. 4131 - 4133 (2001)
Cytochrome P450BM3 and its F87V mutant were exploited for a convenient, laboratory scale (1 mmol) preparation of 14(S),15(R)-epoxyeicosatrienoic acid [14(S),15(R)-EET] from arachidonic acid and (+)-leukotoxin B [(+)-12(S),13(R)-vernolic acid] from linoleic acid, respectively. Their enantiomers were accessed via a four-step chemical inversion.
