1527-15-7 Usage
Molecular structure
Benzene derivative with a chloromethyl group and a phenylthio group attached to the benzene ring
Functional groups
Chloromethyl (-CH2Cl) and phenylthio (-SPh) groups
Appearance
Unknown, but likely a solid or liquid depending on the conditions
Physical state
Unknown, but likely a solid or liquid depending on the conditions
Solubility
Unknown, but likely soluble in organic solvents such as ethanol, acetone, or dichloromethane
Boiling point
Unknown, but can be estimated based on similar compounds
Melting point
Unknown, but can be estimated based on similar compounds
Density
Unknown, but can be estimated based on similar compounds
Reactivity
Reacts with nucleophiles, such as amines, alcohols, and thiols, to form various products
Uses
Building block in organic synthesis, production of pharmaceuticals, dyes, and other chemicals
Safety
Toxic and harmful if ingested, inhaled, or in contact with skin; proper safety measures and protective equipment should be used when handling
Hazardous properties
Potential irritant, corrosive, and harmful if ingested, inhaled, or in contact with skin
Storage
Should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames
Disposal
Dispose of according to local, national, and international regulations for hazardous materials
Environmental impact
Potentially harmful to aquatic life and the environment; proper disposal and handling are essential to minimize environmental impact
Check Digit Verification of cas no
The CAS Registry Mumber 1527-15-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1527-15:
(6*1)+(5*5)+(4*2)+(3*7)+(2*1)+(1*5)=67
67 % 10 = 7
So 1527-15-7 is a valid CAS Registry Number.
1527-15-7Relevant articles and documents
New α-aryl-β,N-imidazolylethyl benzyl and naphthylmethyl ethers with antimycotic and antibacterial activity
Nardi,Cappelletti,Catto,Leonardi,Tajana,Veronese
, p. 2123 - 2126 (2007/10/02)
A new series of α-aryl-β,N-imidazolylethyl benzyl and naphthylmethyl ethers was synthesized and tested for antimycotic and antimicrobial activity. All compounds showed antifungal activity; most of them were also active against gram-positive bacteria, whereas no activity was detected against gram-negative bacteria. Structure-activity relationships are discussed. The α-(2,4-dichlorophenyl)-β,N-imidazolylethyl 4-phenylthiobenzyl ether nitrate (8), which showed good ski tolerability and in vivo antimycotic activity comparable with or better than 1-[2,4-dichloro-β-(2,4-dichlorobenzyloxy)phenethyl]imidazole (miconazole) and 1-[α-(o-chlorophenyl)benzhydryl]imidazole (clotrimazole), was selected for further researches.
