85363-39-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
Dodecene diols are a class of organic compounds that contain a dodecene chain with two hydroxyl (-OH) groups.
Explanation
The compound has a 12-carbon (dodecene) chain with hydroxyl groups attached to the first and ninth carbon atoms.
Explanation
A phenylseleno group, which consists of a phenyl ring (C6H5) with a selenium atom (Se) attached, is present at the tenth carbon atom of the dodecene chain.
Explanation
The hydroxyl group at the first carbon atom is acetylated, meaning it is replaced by an acetyl group (-COCH3), forming an ester linkage.
Explanation
The compound is utilized in organic synthesis as a reagent to prepare various organic compounds.
Explanation
It is also used in chemical research for studying the properties and reactions of similar compounds.
Explanation
The compound may have potential uses in the development of pharmaceuticals and agricultural products due to its unique structure and reactivity.
Explanation
It is a chemical compound, which means it is a substance formed from two or more elements chemically bonded together in a fixed proportion.
Explanation
The compound is composed of these four elements, which contribute to its unique properties and reactivity.
Explanation
Due to the presence of chiral centers (carbon atoms with four different substituents), the compound may have stereoisomers, which are compounds with the same molecular formula but different spatial arrangements of atoms.
Class
Dodecene diols
Structure
Dodecene chain with hydroxyl groups at the 1st and 9th positions
Phenylseleno group
Attached at the 10th position
Acetylation
At the 1st position
Organic synthesis
Used as a reagent
Chemical research
Employed in research
Potential applications
Pharmaceutical and agricultural industries
Chemical compound
Belongs to the category of chemical compounds
Elemental composition
Contains carbon (C), hydrogen (H), oxygen (O), and selenium (Se)
Stereochemistry
Potential for stereoisomers
Check Digit Verification of cas no
The CAS Registry Mumber 85363-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,6 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85363-39:
(7*8)+(6*5)+(5*3)+(4*6)+(3*3)+(2*3)+(1*9)=149
149 % 10 = 9
So 85363-39-9 is a valid CAS Registry Number.
85363-39-9Relevant articles and documents
Regiochemical Convergence in the Reaction of Heterosubstituted Allylic Carbanions via Allylic Aluminum and Boron "Ate" Complexes
Yamamoto, Yoshinori,Yatagai, Hidetaka,Saito, Yoshikazu,Maruyama, Kazuhiro
, p. 1096 - 1104 (2007/10/02)
The regiochemistry in reactions of heterosubstituted allylic carbanions (1) is highly controlled via allylic aluminum or boron "ate" complexes which direct both carbonyl compounds and reactive halides to the α-position with high regioselectivity.For example, carbonyl compounds react with the oxygen- (3), sulfur- (12), selenium- (20), and silicon- (25) substituted allylic carbanions at the α-position via the ate complexes.Although the reactions of the ate complexes (2) with aldehydes generally produce a mixture of erythro and threo isomers, the aluminum ate comlex of 3b gives the erythro isomer (5) with very high stereoselectivity.This procedure is applied to the stereoselective synthesis of exo-brevicomin (9).With allylic halides, the oxygen- (3a) and sulfur- (12) substituted allylic carbanions again react at the α-position via the ate complexes.However, the coupling mode is entirely different; the α-α' coupling product (10) is obtained from 3a, while the α-γ' coupling product (15) is produced from 12.
