127703-37-1 Usage
Chemical composition
Consists of a cyanophenyl (C6H4CN) group and a methylphenol (C7H7O) group attached to the benzene ring.
Cyanophenyl group position
Attached to the 2-position of the benzene ring.
Methylphenol group position
Attached to the 4-position of the benzene ring.
Antibacterial properties
Exhibits the ability to kill or inhibit the growth of bacteria.
Antifungal properties
Demonstrates the capability to destroy or suppress the growth of fungi.
Pharmaceutical applications
Widely studied for its potential use in the development of drugs.
Organic synthesis intermediate
Utilized as a starting compound or stepping stone in the synthesis of more complex organic molecules.
Versatile building block
Its chemical structure allows for the creation of a variety of complex molecules.
Industrial importance
Serves as a key ingredient in multiple industries due to its properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 127703-37-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,0 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 127703-37:
(8*1)+(7*2)+(6*7)+(5*7)+(4*0)+(3*3)+(2*3)+(1*7)=121
121 % 10 = 1
So 127703-37-1 is a valid CAS Registry Number.
127703-37-1Relevant articles and documents
SRN1C-arylation of potassium aryloxides by arylazo phenyl or tert- butyl sulfides in DMSO
Petrillo, Giovanni,Novi, Marino,Dell Erba, Carlo,Tavani, Cinzia,Berta, Giovanni
, p. 7977 - 7990 (2007/10/02)
Aryloxide ions (Ar′O-) behave as C-nucleophiles towards diazosulfides (ArN = NSR; R = Ph, But) leading to imsymmetrical hydroxybiaryls (ArAr′OH) via C-C coupling. The reaction is particularly suited for the synthesis of terms which contain electron-withdrawing groups on the Ar moiety. The SRN1 mechanism is proposed on the grounds of experimental evidences.
