92907-14-7 Usage
Explanation
The compound's full name, which describes its structure and functional groups.
Explanation
An alternative name for the compound, often used in the scientific community.
Explanation
The molecular formula representing the compound's composition, with 16 carbon atoms, 15 hydrogen atoms, 1 chlorine atom, and 1 oxygen atom.
Explanation
The mass of one mole of the compound, calculated from its chemical formula.
Explanation
The compound is derived from propenylbenzene by introducing a chlorine atom.
Explanation
The key functional groups present in the molecule, which contribute to its reactivity and properties.
Explanation
The compound is used as a starting material or intermediate in the production of various drugs and agricultural chemicals.
Explanation
The compound serves as a reagent, participating in various chemical processes due to its reactive functional groups.
Explanation
The compound can be used as a building block to create more complex organic molecules.
Explanation
The presence of these functional groups makes the compound more susceptible to chemical reactions, increasing its utility in various applications.
Molecular Weight
262.75 g/mol
Structure
Chlorinated derivative of propenylbenzene
Functional Groups
Chloro, propenyl, and 4-methylphenoxy
Application
Synthesis of pharmaceuticals and agrochemicals
Use as a Reagent
In chemical reactions
Building Block
Production of other organic compounds
Reactivity
Highly reactive due to chloro and propenyl groups
Check Digit Verification of cas no
The CAS Registry Mumber 92907-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,0 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92907-14:
(7*9)+(6*2)+(5*9)+(4*0)+(3*7)+(2*1)+(1*4)=147
147 % 10 = 7
So 92907-14-7 is a valid CAS Registry Number.
92907-14-7Relevant articles and documents
Catalytic enantioselective aziridoarylation of aryl cinnamyl ethers toward synthesis of trans-3-amino-4-arylchromans
Hajra, Saumen,Sinha, Debarshi
body text, p. 7334 - 7340 (2011/11/06)
Catalytic enantioselective one-pot aziridoarylation reaction of aryl cinnamyl ethers has been demonstrated in detail. Combination of suitable copper catalyst and chiral bis-oxazoline ligand was found to be very efficient for asymmetric aziridination followed by intramolecular arylation (Friedel-Crafts) reaction to provide a general and direct method for the synthesis of trans-3-amino-4-arylchromans with high regio-, diastereo- (dr > 99:1), and enantioselectivity (up to 95% ee) with moderate yield. trans-3-Amino-4- arylchroman is an advanced intermediate for the synthesis of chromenoisoquinoline compounds such as doxanthrine, a potent and selective full agonist for the dopamine-D1 receptor.
Enantioselective and regioselective ruthenium-catalyzed decarboxylative etherification of allyl aryl carbonates
Austeri, Martina,Linder, David,Lacour, Jerome
experimental part, p. 5737 - 5741 (2009/05/31)
A study was conducted to investigate enantioselective and regioselective ruthenium-catalyzed decarboxylative etherification of allyl aryl carbonates. It was observed that allyl aryl carbonates react in the presence of CpRu and pyridylmonooxazoline ligands, to produced branched allyl aryl ethers in high enantiomeric purity and significant regioselectivity. The transformation demonstrated an effective enantioselective decarboxylative etherification. Initial investigations were conducted, using conditions similar to that of the enantioselective rearrangement of allyl β-keto esters. Allyl carbonate was treated with catalytic amounts of CpRu in THF at room temperature. The scope of the asymmetric protocol was also studied with allyl carbonates, with improved conditions.
